Viktor Palmi publikatsioonid

Palm, V.; Palm, N.; Tenno, T. (2006). Computerized database and software for retrieval, processing and prognosis of rate and equilibrium constants of chemical reactions. Proceedings of the Estonian Academy of Sciences. Chemistry, 55(1), 3–13.

Palm, V.; Palm, N.; Tenno, T. (2004). Modification of data processing and interpretation of results related to the use of multiparameter correlation analysis: introduction of additional characteristics and criterias. Part 1. Application to the treatment of solvent effects. Journal of Physical Organic Chemistry, 17(10), 876– 889.

Palm, V.; Kiho, J.; Jalas, A.; Tenno, T.; Palm, N. (2004). Computerized Database on Chemical Reactivity (Rate and Equilibrium Constants) and Concerted Software for Retrieval, Processing, and Prognosis of Data. In: International Conference on Education and Information Systems: Technologies and Applications, vol. 2. Proceedings: International Conference on Education and Information Systems (EISTA ’04); Orlando, USA; 21-25 July, 2004. Orlando, USA: 2004, 190-195.

Palm, V.; Tenno, T.; Palm, N. (2004). Averaged Values and the Problem of Generality for Substituent Constants. In: The Tenth International Conference on Correlation Analysis in Chemistry (CAIC, X): The Tenth International Conference on Correlation Analysis in Chemistry; Busan, Korea; 2004.

Palm, N.; Palm, V. (2001). Verification of the Modified Approach to Solvation Effects on the Basis of Extended Data Set: III. Results of Statistical Data Treatment for Particular Processes. Russian Journal of Organic Chemistry, 37, 935-939.

Jalas, A.; Palm, V.; Tenno, T. (2001). A computerized storage and retrieval system of pKa values of hydrogen acids. Proceedings of the Estonian Academy of Sciences, Chemistry (2001), 50(3), 186-192.

Palm, V. (2001). Some fundamental criteria of the scientific method and the internal structure of science. R.Vihalemm (Editor.). Estonian studies in the history and philosophy of science (91-110). Dordrecht/Boston/London: Kluwer Academic Publishers.

Palm, V.; Jalas, A.; Tenno, T. (2001). pKa Database. Dissociation of Hydrogen Acids (http:/mega.chem.ut.ee/tktool/teadus/pkdb). 1.

Palm, N.; Palm, V. (2000). Verification of modified approach to solvation effects based on extended set of data series II: procedure and verification results of averaged statistical significance of solvent constants scales. Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii), 36(8), 1075-1104.

Palm, V.; Jalas, A.; Kiho, J.; Tenno, T. (1997). A computerized system for storage, processing and prognostication of data with orientation toward the use of correlation equations. Organic Reactivity (Tartu), 31(1), 111-133.

Jalas, A.; Kiho, J.; Palm, V.; Tenno, T. (1997). Data structure and menu-based access of the rate and equilibrium constants of heterolytic organic reactions database. Organic Reactivity (Tartu), 31(1), 135-140.

Palm, N.; Palm, V. (1997). Check of a modified approach to solvent effects by processing of an extended set of solvent-dependent data series. 1. Test of an earlier defined set of nine solvent parameters. Organic Reactivity (Tartu), 31(1), 141-158.

Palm, V.; Timotheus, V.; Pooga, H.; Kaasik, S.; Palm, N. (1996). Reinvestigation of the substituent, environmental, and temperature effects on the solvolysis kinetics of disubstituted Mannich bases of the general structure 3-X1C6H4NHCH2C(NO2)2C6H4X2-3. 1. The set of experimental data. Organic Reactivity (Tartu), 30(1), 69-72.

Palm, V.; Kaasik, S. (1996). Reinvestigation of the substituent, environmental, and temperature effects on the solvolysis kinetics of disubstituted Mannich bases of the general structure 3-X1C6H4NHCH2C(NO2)2C6H4X2-3. 2. Quantitative interpretation of combined substituent, solvent, and temperature effects. Organic Reactivity (Tartu), 30(1), 73-83.

Nummert, V.; Piirsalu, M.; Palm, V. (1996). Kinetic study of hydrolysis of benzoates. XIX. Influence of temperature on ortho effect for water solution. Isokinetic dependence in the case of additional ortho induction effect. Organic Reactivity (Tartu), 30(1), 85-94.

Palm, V. (1995). International Journal on Quantitative Structure-Reactivity and -Property Relations.[In: Org. React. (Tartu).,1995; 29(1)]. Palm, V.; Editor. Estonia, 121 pp. Publisher: (Tartu Univiversity, Tartu, Estonia).

Palm, V. (1995). Isosteric constants found by nonlinear procedure from Menshutkin reaction data. Organic Reactivity (Tartu), 29(1), 37-40.

Matveev, A. A.; Popov, A. F.; Palm, V. A.; Piskunova, Zh. P. (1993). Factors affecting rate of the Menshutkin reaction. 3. Temperature effect. Organic Reactivity (Tartu), 28(1), 35-38.

Nummert, V.; Palm, V. (1993). Kinetic study of alkaline hydrolysis of substituted phenyl tosylates. XX. Influence of temperature on ortho effect. Isokinetic dependence in the case of additional ortho inductive effect. Organic Reactivity (Tartu), 28(1), 63-71.

Nummert, V.; Piirsalu, M.; Palm, V. (1993). Kinetic study of alkaline hydrolysis of substituted phenyl tosylates. XXI. Influence of solvent on the ortho effect. Organic Reactivity (Tartu), 28(1), 82-87.

Leinbock, R.; Palm, V. (1993). Check of electrostatic model for structural effects on formation enthalpies and dipole moments. 1. Algorithm and computer program for calculations in the framework of model of atomic point charges. Organic Reactivity (Tartu), 28(1), 96-100.

Leinbock, R.; Palm, V. (1993). Check of electrostatic model for structural effects on formation enthalpies and dipole moments. 2. Results for alkanes and cycloalkanes, alkenes and alkynes. Organic Reactivity (Tartu), 28(1), 101-109.

Hiob, R.; Palm, V. (1993). Structural and temperature effects in the gas phase hydrogen abstraction reactions from compounds with general structure R-H. 1. Abstraction by hydrogen atom. Organic Reactivity (Tartu), 28(1), 110-118.

Hiob, R.; Palm, V. (1993). Structural and temperature effects in the gas phase hydrogen abstraction reactions from compounds with general structure R-H. 2. Abstraction by variable free radicals. Organic Reactivity (Tartu), 28(1), 119-124.

Palm, V.; Palm, N. (1993). On the total number and list of parameter scales significant for general quantitative description of solvent effects. Organic Reactivity (Tartu) 28(1), 125-150.

Nummert, V.; Piirsalu, M.; Palm, V. (1990). Kinetic study of alkaline hydrolysis of substituted phenyl tosylates. XVIII. Results of kinetic measurements of o-substituted tosylates in 80% aqueous dimethyl sulfoxide. Organic Reactivity (Tartu), 27(3-4), 99-127.

Palm, V. (1990). Computer-managed automatic data retrieval and prognosis system for rate and equilibrium constants of organic reactions. Journal of Chemical Information and Computer Science, 30(4), 409-412.

Palm, V. (Editor), (1990). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Suppl. Vol. 5, 690 pp. Tartu.

Palm, V. (Editor), (1990). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Suppl. Vol. 6, 869 pp. Tartu.

Palm, V. (Editor), (1989). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Suppl. Vol. 2, 714 pp. Tartu.

Palm, V. (Editor), (1989). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Suppl. Vol. 3, 794 pp. Tartu.

Palm, V. (Editor), (1989). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Suppl. Vol. 4, 623 pp. Tartu.

Tuulmets, A.; Horak, M.; Hansen, E.; Palm, V. (1987). Some structure-reactivity relationships for alkyl bromides in the Grignard reaction. Organic Reactivity (Tartu), 24(4), 412-424.

Palm, V.; Musaeva, M. F. (1986). An attempt at quantitative description of combined temperature and solvent effects for diene condensation. Organic Reactivity (Tartu), 23(1), 96-107.

Palm, V. A.; Hiob, R. J. (1986). Quantitative statistical interpretation of kinetic data in the gas phase homolysis. 8. Program for automatic computational estimation of rate constants of gas phase homolysis and heats of formation of covalent compounds. Organic Reactivity (Tartu), 23(4), 412-439.

Sild, V. A.; Palm, V. A.. (1986). Realization of the general algorithm of the solution of direct problems for homogeneous equilibrium-kinetic mechanistic schemes. Organic Reactivity (Tartu), 23(4), 482-506.

Koppel, I. A.; Molder, U. H.; Palm, V. A. (1985). Ab initio SCF LCAO MO calculations of molecules. IV. Proton affinities. Comparison with experiment. Organic Reactivity (Tartu), 22(1), 3-45.

Matveev, A. A.; Piskunova, Zh. P.; Palm, V. A.; Popov, A. F. (1985). Factors affecting rate of Menshutkin reaction. 1. Effect of amine structure. Organic Reactivity (Tartu), 22(1), 110-118.

Palm, N.; Palm, V. (1985). Determination of the kinetic-equilibrium parameters of the reaction of triphenylaluminum with benzophenone. Organic Reactivity (Tartu), 22(2), 131-141.

Popov, A. F.; Matveev, A. A.; Piskunova, Zh. P.; Palm, V. A. (1985). Factors affecting the rate of Menshutkin reaction. 2. Interdependence of reagent structure effects. Organic Reactivity (Tartu), 22(2), 153-161.

Nummert, V.; Eek, M.; Palm, V . (1985).Kinetic study of alkaline hydrolysis of substituted phenyl tosylates. XIV. Discussion of results of kinetic measurements in 80% aqueous dimethyl sulfoxide. Organic Reactivity (Tartu), 22(3), 263-294.

Palm, V. (Editor), (1985). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Suppl. Vol.1(3-5), 1276 pp. Tartu.

Palm, V. (Editor), (1984). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Suppl. Vol.1(1-2), 496 pp. Tartu.

Leinbok, R. A.; Palm, V. (1984). Nonlinear parametrization of equations for atomic spectral terms. 2. Data processing applying the minimization of relative standard deviation in the equation with a reduced number of parameters. Organic Reactivity (Tartu), 21(2), 127-143.

Juriado, T.; Palm, V. (1984). Program package for computer storage and automatic search of correlation equations and for calculation of rate and equilibrium constants. 1. Digital coding system of equations of chemical reactions. Organic Reactivity (Tartu), 21(3), 255-284.

Uri, A.; Tuulmets, A.; Palm, V. (1983). Transesterification of esters of carboxylic acids by titanium alcoholates. II. Transesterification of esters of aromatic acids. Organic Reactivity (Tartu), 20(1), 122-131.

Hiob, R.; Palm, V. (1983). Quantitative statistical interpretation of kinetic data in gas phase homolysis. 3. Calculation of conventional formation enthalpies of free radicals in the approximation of constant effective mean value of log A0 = 14.64. Organic Reactivity (Tartu), 20(2), 151-202.

Palm, V.; Hiob, R. (1983).Quantitative statistical interpretation of kinetic data in the gas phase homolysis. 4. Calculation of conventional formation enthalpies of free radicals based on experimental activation energies, isokinetic and isoentropic models. Organic Reactivity (Tartu), 20(2), 257-274.

Palm, V.; Hiob, R. (1983).Quantitative statistical interpretation of kinetic data in gas-phase homolysis. 5. Correlation of substituent effects on conventional formation enthalpies of substituted methyl radicals proceeding from isoentropic and isokinetic models. Organic Reactivity (Tartu), 20(2), 321-354.

Leinbok, R.; Palm, V. (1983). Nonlinear parametrization of equations for atomic spectral terms. 1. Specification of general character of dependence on orbital-orbital shielding constants. Organic Reactivity (Tartu), 20(3), 373-396.

Hiob, R.; Palm, V. (1983). Quantitative statistical interpretation of kinetic data in gas-phase homolysis. 6. Attempted simultaneous estimation of entropy and enthalpy contributions to free energy of activation. Organic Reactivity (Tartu), 20(3), 405-443.

Palm, V.; Hiob, R. (1982). Quantitative statistical interpretation of kinetic data in gas-phase homolysis. 2. Results of data treatment in the coordinates of the isokinetic relationship. Organic Reactivity (Tartu), 19(1), 120-140.

Palm, V.; Hiob, R. (1981). Structure effects in the kinetics of gas-phase homolysis. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, Tartu, 18(1), 149-168.

Palm, V.; Hiob, R. (1981). Quantitative statistical interpretation of kinetic data on gas-phase homolysis. 1. Refined computation scheme for heats of formation in the gas phase at 0°K. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, Tartu, 18(3), 445-484.

Nummert, V.; Palm, V. (1980). Study of solvent dependence of j°. 1. Statistical data handling. Organic Reactivity (Tartu), 17(3), 292-312.

Nummert, V.; Palm, V. (1980). Study of solvent dependence of r0. 2. Results and discussion. Organic Reactivity (Tartu), 17(3), 331-351.

Korgesaar, A.; Danilov, I.; Palm, V. (1979). Study of the reactivity of substituted bicyclo[2.2.2] octanes. 1. Formulation of the problem. Methods of synthesis of disubstituted derivatives of bicyclo[2.2.2]octane. Organic Reactivity (Tartu), 16(4), 521-528.

Palm, V. (1979). Interpretation of the primary kinetic salt effect. Probl. Khim. Kinet. , 162-179.

Palm, V.; Editor. (1979). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol. 5(2). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 5(2)). 283 pp. Publisher: VINITI, Moscow, USSR.

Karelson, M.; Palm, V. (1978). New model of electric conductivity of strong electrolyte solutions. Teoreticheskaya i Eksperimental’naya Khimiya, 14(6), 781-787.

Linntam, A. A.; Palm, V. A. (1978).The study of possible applications of atomic orbital energy model. 5. Statistical treatment of atomic spectral terms including electronic configurations up to 1s22s22p53d. Organic Reactivity (Tartu), 15(1), 93-123.

Palm, V.; Editor. (1978). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol. 5(1). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 5(1)). 656 pp. Publisher: VINITI, Moscow, USSR.

Riikoja, J.; Timotheus, H.; Palm, V. (1977). Check of experimental data on solvolysis kinetics of Mannich bases X1C6H4NHCH2C(NO2)2C6H4X2 used in parametrization of four-factor polylinear equation with all gross terms. Organic Reactivity (Tartu), 14(4), 507-526.

Palm, V. (1977). Principles of the Quantitative Theory of Organic Reactions. 2nd Ed. (Osnovy Kolichestvennoi Teorii Organicheskikh Reaktsii). 359 pp. Leningrad.

Palm, V.; Editor. (1977). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol. 2(2). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 2(2)). 618 pp. Publisher: VINITI, Moscow, USSR.

Palm, V.; Editor. (1977). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol. 3(1). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 3(1)). 463 pp. Publisher: VINITI, Moscow, USSR.

Palm, V.; Editor. (1977). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol. 3(2). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 3(2)). 591 pp. Publisher: VINITI, Moscow, USSR.

Palm, V.; Editor. (1977). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol. 4(1). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 4(1)). 580 pp. Publisher: VINITI, Moscow, USSR.

Palm, V.; Editor. (1977). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol. 4(2). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 4(2)). 432 pp. Publisher: VINITI, Moscow, USSR.

Palm, V.; Editor. (1976). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol. 2(1). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 2(1). 706 pp. Publisher: VINITI, Moscow, USSR.

Nummert, V.; Palm, V. (1976). Study of the electric conductivity of sodium o-tosyloxybenzoate in aqueous solutions of sodium hydroxide. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 13(1), 75-83.

Palm, V. (1976). Study of the possible applications of a model of atom orbital energies. 3. Evaluation of constants of paired shielding and nonshielding interactions of electrons for orbitals of the second shell. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 13(1), 117-130.

Palm, V. (1976). Study of the possible applications of a model of atom orbital energies. 4. Energetically accurate basis for quantum-chemical calculations and the possible procedure for the latter. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 13(1), 131-139.

Kozlov, V.; Ivanov, A.; Palm, V. (1976). On the ratio of meta and para isomers in equilibrium mixtures of disubstituted benzenes. Organic Reactivity (Tartu), 13(3), 315-327.

Karelson, M.; Palm, V. (1975). Hydrogen bond energy in ice I calculated using the method of electrostatic interactions between partial charges. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(3), 667-677.

Korgesaar, A.; Palm, V. (1975). Kinetics and mechanism of the reaction of hydrogen chloride with absolute aliphatic alcohols. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(3), 697-707.

Horak, M.; Palm, V.; Soogenbits, U. (1975). Kinetics of Grignard reagent formation. 1. Supplementary kinetic parameters and mechanism of the reaction. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(3), 709-719.

Horak, M.; Palm, V.; Soogenbits, U. (1975). Kinetics of Grignard reagent formation. 2. Effect of the solvent and halide on organomagnesium compound formation. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(3), 721-733.

Juriaado, T.; Palm, V. (1975). Dissociation constants of substituted acetic acid derivatives and inductive conductivity of some alicyclic systems in aqueous methanol. Reaktsionnaya Sposobnost Organicheskikh Soedinenii , 12(1), 123-131.

Nummert, V.; Palm, V.; Uudam, M. (1975). Study of the possible applications of the atomic orbital energy model. 2. Determination of pKa values of formocholine and choline chlorides, and bis(diethylamino)methane. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 12(2), 445-456.

Palm, V. (1975). Study of the possible applications of the atomic orbital energy model. I. Modification of the orbital electronegativity concept and bond polarity model. Reaktsionnaya Sposobnost Organicheskikh Soedinenii , 12(2), 457-462.

Palm, V.; Linntam, A. (1975). Empirical dependence of orbital energies on nuclear charge and electronic configuration. The additivity of screening and nonscreening interactions between electrons. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 12(2), 463-474.

Nummert, V.; Palm, V. (1975). Kinetics of the alkaline hydrolysis of substituted phenyl p-toluene sulfonates. IX. Hydrolysis of o-carboxy-substituted phenyl p-toluene sulfonate. Quantitative interpretation of the salt effect using an electrostatic model. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(3), 581-601.

Palm, V.; Editor. (1975). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol.1(1). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 1(1)). 602 pp. Publisher: VINITI, Moscow, USSR.

Palm, V.; Editor. (1975). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol.1(2). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 1(2)). 299 pp. Publisher: VINITI, Moscow, USSR.

Koppel, I.; Karelson, M.; Palm, V. (1974). Common scale of inductive constants, s*, for neutral and charged substituents. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(1), 101-120.

Korgesaar, A.; Palm, V. (1974). Kinetics and mechanism of the reaction of hydrochloric acid with methanol, ethanol, and 1-propanol and conductometry of their respective solutions. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(1), 141-151.

Karelson, M.; Palm, V.; Hiob, R.; Haldna, U. (1974). Ionization mechanism of strong acids. Trichloroacetic, 2,4,6-trinitrobenzoic, and picric acids in aqueous sulfuric acid. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(1), 239-256.

Palm, V.; Karelson, M. (1974). New model for solutions of electrolytes. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(1), 263-268.

Talvik, I.; Palm, V. (1974). Attempt to interpret acidity of carbon acids using j-constants of substituents. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(2), 287-302.

Palm, V.; Korgesaar, A. (1974). Kinetic detection of conducting and nonconducting ion pairs in reactions of hydrogen chloride with methanol and ethanol. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(2), 523-537.

Karelson, M.; Haldna, U.; Palm, V. (1973). Common relation of the equivalent conductivity of complexes of a proton with oxonium bases and of the hydrated proton itself to their molecular size. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(1), 163-174.

Palm, V.; Nummert, V.; Pussa, T.; Karelson, M.; Koppel, I. (1973). Electrostatic contribution to polar effects of charged substituents and nature of primary salt effect. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(1), 223-242.

Palm, V.; Pussa, T.; Nummert, V.; Talvik, I. (1973). Kinetics of the hydrolysis of benzoates. IV. Polar effects of substituents in the alkyl part. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(1), 243-267.

Karelson, M.; Palm, V.; Haldna, U. (1973). Complexing of nitrosubstituted benzenes with proton in aqueous solutions of sulfuric acid studied by differential conductometry. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(1), 307-322.

Karelson, M.; Palm, V.; Haldna, U. (1973). Differential-conductometric study of the Hammett indicator 2,4-dinitroaniline. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(1), 323-331.

Palm, V.; Palm, N. (1973). Electrostatic model of intramolecular interactions. I. Basic principles and their application to formation enthalpies of alkanes, cyclohexane, and adamantane. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(2), 391-412.

Palm, V. (1973). Electrostatic model of intramolecular interactions. 2. Application to formation enthalpies of fluorine derivatives of methane, some oxygen-containing compounds, and methylamine. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(2), 413-428.

Koppel, I.; Karelson, M. M.; Palm, V. (1973). Demonstration of the universality of the constant a of inductive interaction. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(2), 497-514.

Istomin, B. I.; Palm, V. (1973). Application of the principle of polylinearity to standard thermodynamic characteristics of organic compounds. 8. Compounds with polyvalent functional groups such as -S-, -O-, -S(O),-n<,>NN,< and -00-(of bridging systems). Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(2), 537-565.

Istomin, B. I.; Palm, V. (1973). Application of the principle of polylinearity to standard thermodynamic characteristics of organic compounds. 9. Compounds with the polyvalent functional groups carbon-carbon triple and carbon-carbon and carbon–oxygen double bonds. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(2), 567-582.

Istomin, B. I.; Palm, V. (1973). Application of the principle of polylinearity to standard thermodynamic characteristics of organic compounds. 10. Formation enthalpies of polyfunctional derivatives of alkanes. Separation of the inductive term. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(2), 583-607.

Isotmin, B. I.; Palm, V.; Nummert, V. (1973). Kinetics of alkaline hydrolysis of m-and p- substituted phenyl acetates and ethyl benzoates. Reaktsionnaya Sposobnost Organicheskikh Soedinenii), 10(2), 609-616.

Istomin, B. I.; Palm, V. (1973). Application of the principle of polylinearity to standard thermodynamic characteristics of organic compounds. 11. One variant of a calculation diagram for polysubstituted derivatives of alkanes. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(4), 1005-1010.

Istomin, B. I.; Palm, V. (1973). Application of the principle of polylinearity to standard thermodynamic characteristics of organic compounds. 12. Separation of the resonance interaction term from the enthalpy of formation D Hf0. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(4), 1011-1024.

Istomin, B. I.; Palm, V. (1973). Application of the principle of polylinearity to standard thermodynamic characteristics of formation of RXj compounds. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(4), 1025-1028.

Palm, V.; Haldna, U.; Koppel, I. (1973). Acidity functions and solvation interactions. Reaktsionnaya Sposobnost Organicheskikh Soedineni, 10(4), 1029-1042.

Istomin, B. I.; Palm, V. (1972). Application of PPL [partial linearity principle] to standard thermodynamic characteristics of organic compounds. 2. Structural dependence of jRi constants on sets of constants joRi, jooRi, and FRi for alkyl substituents. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(2), 433-467.

Istomin, B. I.; Palm, V. (1972). Application of PPL to standard thermodynamic characteristics of organic compounds. 3. Enthalpies of formation of monosubstituted alkenes RiX with univalent saturated functional groups mercapto, amino, hydroxyl, chloro, bromo, iodo, and fluoro. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(2), 469-511.

Pussa, T.; Nummert, V.; Palm, V. (1972). Kinetics of hydrolysis of benzoates. I. Alkaline hydrolysis of substituted phenyl benzoates in water. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(3), 697-728.

Karelson, M.; Palm, V.; Haldna, U. (1972). Experimental proof of the constancy of hydrogen ion mobility in the sulfuric acid-water system and substantiation of the applicability of differential conductometric methods in studies of protolytic equilibriums. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(3), 831-846.

Istomin, B. I.; Palm, V. (1972). Application of PPL to standard thermodynamic characteristics of organic compounds. 4. Enthalpies of formation of monosubstituted alkanes RX with univalent functional groups CHO, COOH, CN, ONO2, NO2, CR = CH, C = CH, and C6H5. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(3), 847-870.

Pussa, T.; Nummert, V.; Palm, V. (1972). Kinetics of hydrolysis of benzoates. II. Alkaline hydrolysis of alkyl benzoates in water. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(3), 871-889.

Istomin, B. I.; Palm, V. (1972). Application of PPL to standard thermodynamic characteristics of organic compounds. 5. Contribution of hyperconjugative interaction between the alkyl groupand electron-deficient substituent to the enthalpy of the formation of RiX. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(4), 1089-1104.

Istomin, B. I.; Palm, V. (1972). Application of PPL to standard thermodynamic characteristics of organic compounds. 6. Analysis of the scheme for quantitative correlation with inductive and hyperconjugative contributions of standard formation enthalpies DH.deg.f(298.deg.K,g). Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(4), 1105-1128.

Pussa, T.; Palm, V. (1972). Kinetics of hydrolysis of benzoates. III. Acid hydrolysis of benzoates in water. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(4), 1209-1224.

Istomin, B. I.; Palm, V. (1972). Application of PPL to standard thermodynamic characteristics of organic compounds. 7. Isoparametric relation (Compensation effects) of thermodynamic functions for homologous series of compounds H(CH2)nX X = methyl, phenyl, vinyl, ethynyl, mercaptyl. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(4), 1225-1253.

Koppel, I.; Palm, V. (1972). Influence of the solvent on organic reactivity. Editor(s): Chapman, N. B. Advan. Linear Free Energy Relat. 203-280. Publisher: Plenum Publ. Co. Ltd., London, England.

Maremae, V.; Pussa, T.; Palm, V. (1971). Kinetics of alkaline hydrolysis of substituted phenyl p-toluenesulfonates. VI. Influence of ionic strength of the medium of hydrolysis rate of o-, m-, and p-N(CH3)3+-substituted phenyl p-toluenesulfonates. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 8(1), 127-151.

Koppel, I.; Palm, V. (1971). General equation for solvent effects. Reaktsionnaya Sposobnost Organicheskikh Soedinenii , 8(1), 291-301.

Talvik, I.; Palm, V. (1971). Additional values for steric substituent constants and check of the isostericity principle. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 8(2), 445-462.

Maremae, V.; Palm, V. (1971). Kinetics of alkaline hydrolysis of substituted phenyl p-toluenesulfonates. VII. Deviations from the Debye-Hueckel theory of the influence of ionic strength on alkaline hydrolysis rates for o-, m- and p-hydroxyphenyl p-toluenesulfonates in water. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 8(2), 591-618.

Aaviksaar, A.; Paris, J.; Palm, V. (1971). Relation between catalysis and binding in chymotrypsin reactions. Reaktsionnaya . Sposobnost Organicheskikh Soedinenii, 8(3), 817-832.

Istomin, B. I.; Palm, V. (1971). Thermochemical bond energies and mathematical equivalence of 1,3- and 1,4-schemes for nonbonded interactions in alkanes. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 8(3), 833-844.

Istomin, B. I.; Palm, V. (1971). Application of the partial linearity principle to standard thermodynamic characteristics of organic compounds. I. Equation for monosubstituted alkanes and testing its applicability to thiols and primary amines. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 8(3), 845-866.

Rodima, T. K.; Haldna, U.; Palm, V. (1971). Corrected values of the HM acidity function for aqueous sulfuric acid solutions. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 8(4), 1165-1187.

Rodima, T. K.; Haldna, U.; Palm, V. (1971), Physical meaning of the HMandHR acidity functions. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 8(4), 1189-1199.

Palm, V.; Lebedeva, N. D. (1970). Combination of the additivity principle with LFER for calculating enthalpies of formation of organic compounds. III. Accounting for conformational interactions in amines and substituted hydrazines and estimation of additive contributions of nitrogen-hydrogen, carbon-nitrogen, and nitrogen-nitrogen. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 7(2), 305-336.

Palm, V.; Juriaado, T. (1970). Unsuitability of the simple Broensted scheme for dissociation of trichloroacetic acid. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 7(2), 449-457.

Sikk, P.; Aaviksaar, A.; Godovikov, N. N.; Morozova, N. A.; Palm, V. (1970). Interaction of organophosphorus compounds with a-chymotrypsin. VI. Antichymotrypsin activity of O-ethyl-5-(w-ethylthioalkyl)-methylthiophosphonates and their methylsulfomethylates.Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 7(4), 986-1001.

Palm, V.; Lebedeva, N. D. (1969). Combination of the additivity principle with [linear free energy relationships] for calculation of enthalpies of formation of organic compounds. I. Specifying additives and calculation of conformational contributions for alkanes. Reaktsionnaya Sposobnost Organicheskikh Soedinenii 6(1), 61-83.

Lebedeva, N. D.; Palm, V.; Gutner, N. M. (1969). Combination of the additivity principle with LFER [linear free energy relationship] for calculation of enthalpies of formation of organic compounds. II. Correlation of inductive terms and estimation of the value of the universal constant of inductive interaction. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 6(1), 84-113.

Palm, V.; Istomin, B. I. (1969). Isoparametric relations. Generalization of isokinetic and analogous relations. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 6(2), 427-441.

Koppel, I.; Palm, V. (1969). Dependence of rate constants on the nature and composition of the solvent. XV. Quantitative empirical solvent polarity index on the basis of the formal theory of interaction. Reaktsionnaya Sposobnost Organicheskikh Soedineni, 6(2), 504-526.

Istomin, B. I.; Palm, V. (1969). Expediency of correlations using solvatochromic shifts. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 6(3), 710-719.

Palm, V. (1968). Absence of electrostatic interaction through the molecule frame. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 5(3), 583-600.

Haldna, U.; Palm, V. (1968). Using the additivity of pKa values for polysubstituted anilines during a study of the acidity of strongly-acid media. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 5(4), 965-977.

Haldna, U.; Kuura, H.; Tamme, M.; Palm, V. (1968). Kinetics of the bromination of 3-pentanone in aqueous sulfuric acid solutions. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 5(4), 1009-1032.

Aaviksaar, A.; Nolvak, I.; Palm, V. (1968). Mechanism of reactions of a-chymotrypsin with O-ethyl (p-nitrophenylethyl)phosphonate. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 5(4), 1053-1058.

Neimysheva, A.A.; Palm, V.A.; Semin, G.K.; Loshadkin, N.A.; Knunyants, I.L. (1967). Nucleophilic substitution in derivatives of phosphorus acids. 2. Relation between structure of phosphorus-containing compounds and reactivity – application of correlation equations. Journal of General Chemistry USSR, 37(10), 2140.

Palm, V. (1967). Principles of the Quantitative Theory of Organic Reactions. (Osnovy Kolichestvennoi Teorii Organicheskikh Reaktsii) 356 pp. Publisher: Khimiya, Leningrad.

Palm, V.; Neimysheva, A. A.; Knunyants, I. L. (1967). Correlation[of the neutral hydrolysis rates of dialkylphosphinic acid chlorides with the substituent constants. An unusual dependence[on the steric effects and hyperconjugation. Reaktsionnaya Sposobnost Organicheskikh Soedinenii), 4(1), 38-45.

Koppel, I.; Palm, V. (1967). Dependence of the activity coefficients and the rate constants on the nature and the composition of the solvent. XII. Relations between medium effects and the structure of the solvent molecules using the substituent constants. Reaktsionnaya Sposobnost Organicheskikh Soedineni, 4(2), 381-409.

Pyldoya, P. K.; Palm, V. (1967). The dependence of the ionization potentials of alkyl-substituted aliphatic derivatives on the induction constants and hyperconjugation. A new electronic effect of high intensity. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 4(4), 786-813.

Koppel, I.; Palm, V. (1967). Effect of the nature and composition of the solvent on rate constants. XIII. Use of the “dielectric” theory for calculating the effect of solvent on the solvolysis of tert-butyl chloride in individual (one-component) solvents. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 4(4), 862-891.

Koppel, I.; Palm, V. (1967). Effect of the nature and composition of the solvent on rate constants. XIV. Use of the “dielectric” approach for correlation of the effects of the medium on the solvolysis rate for tert-butyl chloride in binary solvents. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 4(4), 892-911.

Tamme, M.; Kuura, H.; Haldna, U.; Palm, V. (1967). Basicity of diethyl ketone. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 4(4), 912-919.

Palm, V.; Haldna, U.; Talvik, A. (1966). Basicity of carbonyl compounds. Chemistry of the Carbonyl Group, 421-460.

Talvik, I.; Palm, V. (1965). Kinetics and mechanism of the acid catalyzed hydrolysis of esters in water. II. Investigation of esters with electronegative groups in the acyl part. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 2(1), 110-121.

Aaviksaar, A.; Ilomets, T.; Palm, V. (1965). Kinetics and mechanism of enzymic catalysis. Influence of snake venoms on the hydrolysis rate of p-nitrophenyl acetate. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 2(1), 222-238.

Palm, V. (1965). Problem of the transmission of the inductive effect and of polar resonance through rings. Reaktsionnaya Sposobnost. Organicheskikh Soedinenii, 2(2), 123-134.

Haldna, U.; Kuura, H.; Erreline, L.; Palm, V. (1965). Kinetics of the bromination of acetone in aqueous solutions of sulfuric acid. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 2(2), 194-210.

Maremae, V.; Palm, V. (1965). Kinetics of the alkaline hydrolysis of substituted phenyl esters of toluenesulfonic acid. IV. Temperature dependence in the water solution. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 2(3), 209-227.

Palm, V. (1964). Dependence of the rate constants on the nature and the composition of solvent. I. General theory. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 1(1), 128-139.

Palm, V.; Korgesaar, A. (1964). Dependence of the rate constants on the nature and the composition of solvent. II. Application of the general theory in the case of the solvolysis of tertiary-BuCl in mixtures of alcs. with C6H6 and nitrobenzene and in mixts. of C6H6 and nitrobenzene. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 1(1), 140-169.

Koppel, I.; Palm, V. (1964). Dependence of the rate constants on the nature and the composition of solvent. III. Conductimetric investigation of the kinetics of very slow reactions. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 1(1), 170-183.

Maremae, V.; Palm, V. (1964). Kinetics of the alkaline hydrolysis of substituted phenyl esters of p-toluenesulfonic acid. I. Precise estimation of the induction constants s0. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 1(2), 85-102.

Koppel, I.; Korgessaar, A.; Palm, V. (1964). Dependence of the rate constants on the nature and composition of solvent. IV. Mechanism of solvolysis of tert-butyl chloride under electrophilic catalysis. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 1(2), 125-147.

Palm, V.; Korgesaar, A. (1964). Dependence of rate constants on the nature and composition of a solvent. VI. Reaction between HCl and aliphatic alcohols in alcohol-benzene and alcohol-nitrobenzene mixtures. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 1(2), 157-170.

Palm, V. (1963). Some practical problems of the use of correlation equations. Tr. Konf. po Probl. Primeneniya Korrelyatsion. Uravnenii v Organ. Khim., Tartusk. Gos. Univ., Tartu, 1962 ,Volume 2, 136-141.

Palm, V.A.; Vizgert, R.V. (1962). Correlation of rate constants in alkaline hydrolysis of aromatic sulfoacid esters, as dependent on structur of these compounds. Doklady Akademii Nauk SSSR, 142(5), 1091-1094.

Korgesaar, A.; Timotheus, V.; Palm, V. (1962). Dependence of the rate of reaction between alcohols and hydrochloric acid on the composition of the solvent. Tr. Konf. po Probl. Primeneniya Korrelyatsion. Uravnenii v Organ. Khim., Tartusk. Gos. Univ., Tartu, 265-282.

Palm, V.; Haldna, U.; Talvik, A.; Mei, A. (1962). Problems in connection with the protonation of carbonyl compounds and the mechanism of the acid hydrolysis of esters. Uch. Zap. Tartusk. Gos. Univ., No. 127, 91-96.

Palm, V.; Haldna, U.; Talvik, A.; Mei, A . (1962). Protonization of carbonyl compounds and the mechanism of acid hydrolysis of complex esters. Zhurnal Fizicheskoi Khimii , 36, 2499-2501.

Palm, V.A. (1961). Structure and reactivity of organic compounds (quantitative laws). Russian Chemical Reviews, 30(9), 471-498.

Kozlova, K.R.; Palm, V.A. (1961). Synthesis of tetraphenylboronsodium in a tetrahydrofuran solution. Zhurnal Obshchei Khimii, 31(9), 2922.

Haldna, U.; Palm, V. A. (1960). Reduction of basicities to a single standard state. Basicity of acetone. Doklady Akademii Nauk SSSR, 135, 667-670.

Talvik, A.J.; Palm, V.A. (1959). Reactive ability of anions of some carboxylic acids in the acid-catalysed enolization of acetone. Doklady Akademii Nauk SSSR, 129(6), 1349-1352.

Talvik, A.I.; Palm, V.A. (1959). Studies on the kinetics and mechanism of acid hydrolysis of ethyl acetate. Zhurnal Fizicheskoi Khimii, 33(6), 1214-1220.

Palm, V.; Palm, N.; Tenno, T. (2006). Computerized database and software for retrieval, processing and prognosis of rate and equilibrium constants of chemical reactions. Proceedings of the Estonian Academy of Sciences. Chemistry, 55(1), 3–13.

Palm, V.; Palm, N.; Tenno, T. (2004). Modification of data processing and interpretation of results related to the use of multiparameter correlation analysis: introduction of additional characteristics and criterias. Part 1. Application to the treatment of solvent effects. Journal of Physical Organic Chemistry, 17(10), 876– 889.

Palm, V.; Kiho, J.; Jalas, A.; Tenno, T.; Palm, N. (2004). Computerized Database on Chemical Reactivity (Rate and Equilibrium Constants) and Concerted Software for Retrieval, Processing, and Prognosis of Data. In: International Conference on Education and Information Systems: Technologies and Applications, vol. 2. Proceedings: International Conference on Education and Information Systems (EISTA ’04); Orlando, USA; 21-25 July, 2004. Orlando, USA: 2004, 190-195.

Palm, V.; Tenno, T.; Palm, N. (2004). Averaged Values and the Problem of Generality for Substituent Constants. In: The Tenth International Conference on Correlation Analysis in Chemistry (CAIC, X): The Tenth International Conference on Correlation Analysis in Chemistry; Busan, Korea; 2004.

Palm, N.; Palm, V. (2001). Verification of the Modified Approach to Solvation Effects on the Basis of Extended Data Set: III. Results of Statistical Data Treatment for Particular Processes. Russian Journal of Organic Chemistry, 37, 935-939.

Jalas, A.; Palm, V.; Tenno, T. (2001). A computerized storage and retrieval system of pKa values of hydrogen acids. Proceedings of the Estonian Academy of Sciences, Chemistry (2001), 50(3), 186-192.

Palm, V. (2001). Some fundamental criteria of the scientific method and the internal structure of science. R.Vihalemm (Editor.). Estonian studies in the history and philosophy of science (91-110). Dordrecht/Boston/London: Kluwer Academic Publishers.

Palm, V.; Jalas, A.; Tenno, T. (2001). pKa Database. Dissociation of Hydrogen Acids (http:/mega.chem.ut.ee/tktool/teadus/pkdb). 1.

Palm, N.; Palm, V. (2000). Verification of modified approach to solvation effects based on extended set of data series II: procedure and verification results of averaged statistical significance of solvent constants scales. Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii), 36(8), 1075-1104.

Palm, V.; Jalas, A.; Kiho, J.; Tenno, T. (1997). A computerized system for storage, processing and prognostication of data with orientation toward the use of correlation equations. Organic Reactivity (Tartu), 31(1), 111-133.

Jalas, A.; Kiho, J.; Palm, V.; Tenno, T. (1997). Data structure and menu-based access of the rate and equilibrium constants of heterolytic organic reactions database. Organic Reactivity (Tartu), 31(1), 135-140.

Palm, N.; Palm, V. (1997). Check of a modified approach to solvent effects by processing of an extended set of solvent-dependent data series. 1. Test of an earlier defined set of nine solvent parameters. Organic Reactivity (Tartu), 31(1), 141-158.

Palm, V.; Timotheus, V.; Pooga, H.; Kaasik, S.; Palm, N. (1996). Reinvestigation of the substituent, environmental, and temperature effects on the solvolysis kinetics of disubstituted Mannich bases of the general structure 3-X1C6H4NHCH2C(NO2)2C6H4X2-3. 1. The set of experimental data. Organic Reactivity (Tartu), 30(1), 69-72.

Palm, V.; Kaasik, S. (1996). Reinvestigation of the substituent, environmental, and temperature effects on the solvolysis kinetics of disubstituted Mannich bases of the general structure 3-X1C6H4NHCH2C(NO2)2C6H4X2-3. 2. Quantitative interpretation of combined substituent, solvent, and temperature effects. Organic Reactivity (Tartu), 30(1), 73-83.

Nummert, V.; Piirsalu, M.; Palm, V. (1996). Kinetic study of hydrolysis of benzoates. XIX. Influence of temperature on ortho effect for water solution. Isokinetic dependence in the case of additional ortho induction effect. Organic Reactivity (Tartu), 30(1), 85-94.

Palm, V. (1995). International Journal on Quantitative Structure-Reactivity and -Property Relations.[In: Org. React. (Tartu).,1995; 29(1)]. Palm, V.; Editor. Estonia, 121 pp. Publisher: (Tartu Univiversity, Tartu, Estonia).

Palm, V. (1995). Isosteric constants found by nonlinear procedure from Menshutkin reaction data. Organic Reactivity (Tartu), 29(1), 37-40.

Matveev, A. A.; Popov, A. F.; Palm, V. A.; Piskunova, Zh. P. (1993). Factors affecting rate of the Menshutkin reaction. 3. Temperature effect. Organic Reactivity (Tartu), 28(1), 35-38.

Nummert, V.; Palm, V. (1993). Kinetic study of alkaline hydrolysis of substituted phenyl tosylates. XX. Influence of temperature on ortho effect. Isokinetic dependence in the case of additional ortho inductive effect. Organic Reactivity (Tartu), 28(1), 63-71.

Nummert, V.; Piirsalu, M.; Palm, V. (1993). Kinetic study of alkaline hydrolysis of substituted phenyl tosylates. XXI. Influence of solvent on the ortho effect. Organic Reactivity (Tartu), 28(1), 82-87.

Leinbock, R.; Palm, V. (1993). Check of electrostatic model for structural effects on formation enthalpies and dipole moments. 1. Algorithm and computer program for calculations in the framework of model of atomic point charges. Organic Reactivity (Tartu), 28(1), 96-100.

Leinbock, R.; Palm, V. (1993). Check of electrostatic model for structural effects on formation enthalpies and dipole moments. 2. Results for alkanes and cycloalkanes, alkenes and alkynes. Organic Reactivity (Tartu), 28(1), 101-109.

Hiob, R.; Palm, V. (1993). Structural and temperature effects in the gas phase hydrogen abstraction reactions from compounds with general structure R-H. 1. Abstraction by hydrogen atom. Organic Reactivity (Tartu), 28(1), 110-118.

Hiob, R.; Palm, V. (1993). Structural and temperature effects in the gas phase hydrogen abstraction reactions from compounds with general structure R-H. 2. Abstraction by variable free radicals. Organic Reactivity (Tartu), 28(1), 119-124.

Palm, V.; Palm, N. (1993). On the total number and list of parameter scales significant for general quantitative description of solvent effects. Organic Reactivity (Tartu) 28(1), 125-150.

Nummert, V.; Piirsalu, M.; Palm, V. (1990). Kinetic study of alkaline hydrolysis of substituted phenyl tosylates. XVIII. Results of kinetic measurements of o-substituted tosylates in 80% aqueous dimethyl sulfoxide. Organic Reactivity (Tartu), 27(3-4), 99-127.

Palm, V. (1990). Computer-managed automatic data retrieval and prognosis system for rate and equilibrium constants of organic reactions. Journal of Chemical Information and Computer Science, 30(4), 409-412.

Palm, V. (Editor), (1990). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Suppl. Vol. 5, 690 pp. Tartu.

Palm, V. (Editor), (1990). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Suppl. Vol. 6, 869 pp. Tartu.

Palm, V. (Editor), (1989). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Suppl. Vol. 2, 714 pp. Tartu.

Palm, V. (Editor), (1989). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Suppl. Vol. 3, 794 pp. Tartu.

Palm, V. (Editor), (1989). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Suppl. Vol. 4, 623 pp. Tartu.

Tuulmets, A.; Horak, M.; Hansen, E.; Palm, V. (1987). Some structure-reactivity relationships for alkyl bromides in the Grignard reaction. Organic Reactivity (Tartu), 24(4), 412-424.

Palm, V.; Musaeva, M. F. (1986). An attempt at quantitative description of combined temperature and solvent effects for diene condensation. Organic Reactivity (Tartu), 23(1), 96-107.

Palm, V. A.; Hiob, R. J. (1986). Quantitative statistical interpretation of kinetic data in the gas phase homolysis. 8. Program for automatic computational estimation of rate constants of gas phase homolysis and heats of formation of covalent compounds. Organic Reactivity (Tartu), 23(4), 412-439.

Sild, V. A.; Palm, V. A.. (1986). Realization of the general algorithm of the solution of direct problems for homogeneous equilibrium-kinetic mechanistic schemes. Organic Reactivity (Tartu), 23(4), 482-506.

Koppel, I. A.; Molder, U. H.; Palm, V. A. (1985). Ab initio SCF LCAO MO calculations of molecules. IV. Proton affinities. Comparison with experiment. Organic Reactivity (Tartu), 22(1), 3-45.

Matveev, A. A.; Piskunova, Zh. P.; Palm, V. A.; Popov, A. F. (1985). Factors affecting rate of Menshutkin reaction. 1. Effect of amine structure. Organic Reactivity (Tartu), 22(1), 110-118.

Palm, N.; Palm, V. (1985). Determination of the kinetic-equilibrium parameters of the reaction of triphenylaluminum with benzophenone. Organic Reactivity (Tartu), 22(2), 131-141.

Popov, A. F.; Matveev, A. A.; Piskunova, Zh. P.; Palm, V. A. (1985). Factors affecting the rate of Menshutkin reaction. 2. Interdependence of reagent structure effects. Organic Reactivity (Tartu), 22(2), 153-161.

Nummert, V.; Eek, M.; Palm, V . (1985).Kinetic study of alkaline hydrolysis of substituted phenyl tosylates. XIV. Discussion of results of kinetic measurements in 80% aqueous dimethyl sulfoxide. Organic Reactivity (Tartu), 22(3), 263-294.

Palm, V. (Editor), (1985). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Suppl. Vol.1(3-5), 1276 pp. Tartu.

Palm, V. (Editor), (1984). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Suppl. Vol.1(1-2), 496 pp. Tartu.

Leinbok, R. A.; Palm, V. (1984). Nonlinear parametrization of equations for atomic spectral terms. 2. Data processing applying the minimization of relative standard deviation in the equation with a reduced number of parameters. Organic Reactivity (Tartu), 21(2), 127-143.

Juriado, T.; Palm, V. (1984). Program package for computer storage and automatic search of correlation equations and for calculation of rate and equilibrium constants. 1. Digital coding system of equations of chemical reactions. Organic Reactivity (Tartu), 21(3), 255-284.

Uri, A.; Tuulmets, A.; Palm, V. (1983). Transesterification of esters of carboxylic acids by titanium alcoholates. II. Transesterification of esters of aromatic acids. Organic Reactivity (Tartu), 20(1), 122-131.

Hiob, R.; Palm, V. (1983). Quantitative statistical interpretation of kinetic data in gas phase homolysis. 3. Calculation of conventional formation enthalpies of free radicals in the approximation of constant effective mean value of log A0 = 14.64. Organic Reactivity (Tartu), 20(2), 151-202.

Palm, V.; Hiob, R. (1983).Quantitative statistical interpretation of kinetic data in the gas phase homolysis. 4. Calculation of conventional formation enthalpies of free radicals based on experimental activation energies, isokinetic and isoentropic models. Organic Reactivity (Tartu), 20(2), 257-274.

Palm, V.; Hiob, R. (1983).Quantitative statistical interpretation of kinetic data in gas-phase homolysis. 5. Correlation of substituent effects on conventional formation enthalpies of substituted methyl radicals proceeding from isoentropic and isokinetic models. Organic Reactivity (Tartu), 20(2), 321-354.

Leinbok, R.; Palm, V. (1983). Nonlinear parametrization of equations for atomic spectral terms. 1. Specification of general character of dependence on orbital-orbital shielding constants. Organic Reactivity (Tartu), 20(3), 373-396.

Hiob, R.; Palm, V. (1983). Quantitative statistical interpretation of kinetic data in gas-phase homolysis. 6. Attempted simultaneous estimation of entropy and enthalpy contributions to free energy of activation. Organic Reactivity (Tartu), 20(3), 405-443.

Palm, V.; Hiob, R. (1982). Quantitative statistical interpretation of kinetic data in gas-phase homolysis. 2. Results of data treatment in the coordinates of the isokinetic relationship. Organic Reactivity (Tartu), 19(1), 120-140.

Palm, V.; Hiob, R. (1981). Structure effects in the kinetics of gas-phase homolysis. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, Tartu, 18(1), 149-168.

Palm, V.; Hiob, R. (1981). Quantitative statistical interpretation of kinetic data on gas-phase homolysis. 1. Refined computation scheme for heats of formation in the gas phase at 0°K. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, Tartu, 18(3), 445-484.

Nummert, V.; Palm, V. (1980). Study of solvent dependence of j°. 1. Statistical data handling. Organic Reactivity (Tartu), 17(3), 292-312.

Nummert, V.; Palm, V. (1980). Study of solvent dependence of r0. 2. Results and discussion. Organic Reactivity (Tartu), 17(3), 331-351.

Korgesaar, A.; Danilov, I.; Palm, V. (1979). Study of the reactivity of substituted bicyclo[2.2.2] octanes. 1. Formulation of the problem. Methods of synthesis of disubstituted derivatives of bicyclo[2.2.2]octane. Organic Reactivity (Tartu), 16(4), 521-528.

Palm, V. (1979). Interpretation of the primary kinetic salt effect. Probl. Khim. Kinet. , 162-179.

Palm, V.; Editor. (1979). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol. 5(2). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 5(2)). 283 pp. Publisher: VINITI, Moscow, USSR.

Karelson, M.; Palm, V. (1978). New model of electric conductivity of strong electrolyte solutions. Teoreticheskaya i Eksperimental’naya Khimiya, 14(6), 781-787.

Linntam, A. A.; Palm, V. A. (1978).The study of possible applications of atomic orbital energy model. 5. Statistical treatment of atomic spectral terms including electronic configurations up to 1s22s22p53d. Organic Reactivity (Tartu), 15(1), 93-123.

Palm, V.; Editor. (1978). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol. 5(1). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 5(1)). 656 pp. Publisher: VINITI, Moscow, USSR.

Riikoja, J.; Timotheus, H.; Palm, V. (1977). Check of experimental data on solvolysis kinetics of Mannich bases X1C6H4NHCH2C(NO2)2C6H4X2 used in parametrization of four-factor polylinear equation with all gross terms. Organic Reactivity (Tartu), 14(4), 507-526.

Palm, V. (1977). Principles of the Quantitative Theory of Organic Reactions. 2nd Ed. (Osnovy Kolichestvennoi Teorii Organicheskikh Reaktsii). 359 pp. Leningrad.

Palm, V.; Editor. (1977). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol. 2(2). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 2(2)). 618 pp. Publisher: VINITI, Moscow, USSR.

Palm, V.; Editor. (1977). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol. 3(1). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 3(1)). 463 pp. Publisher: VINITI, Moscow, USSR.

Palm, V.; Editor. (1977). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol. 3(2). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 3(2)). 591 pp. Publisher: VINITI, Moscow, USSR.

Palm, V.; Editor. (1977). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol. 4(1). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 4(1)). 580 pp. Publisher: VINITI, Moscow, USSR.

Palm, V.; Editor. (1977). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol. 4(2). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 4(2)). 432 pp. Publisher: VINITI, Moscow, USSR.

Palm, V.; Editor. (1976). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol. 2(1). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 2(1). 706 pp. Publisher: VINITI, Moscow, USSR.

Nummert, V.; Palm, V. (1976). Study of the electric conductivity of sodium o-tosyloxybenzoate in aqueous solutions of sodium hydroxide. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 13(1), 75-83.

Palm, V. (1976). Study of the possible applications of a model of atom orbital energies. 3. Evaluation of constants of paired shielding and nonshielding interactions of electrons for orbitals of the second shell. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 13(1), 117-130.

Palm, V. (1976). Study of the possible applications of a model of atom orbital energies. 4. Energetically accurate basis for quantum-chemical calculations and the possible procedure for the latter. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 13(1), 131-139.

Kozlov, V.; Ivanov, A.; Palm, V. (1976). On the ratio of meta and para isomers in equilibrium mixtures of disubstituted benzenes. Organic Reactivity (Tartu), 13(3), 315-327.

Karelson, M.; Palm, V. (1975). Hydrogen bond energy in ice I calculated using the method of electrostatic interactions between partial charges. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(3), 667-677.

Korgesaar, A.; Palm, V. (1975). Kinetics and mechanism of the reaction of hydrogen chloride with absolute aliphatic alcohols. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(3), 697-707.

Horak, M.; Palm, V.; Soogenbits, U. (1975). Kinetics of Grignard reagent formation. 1. Supplementary kinetic parameters and mechanism of the reaction. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(3), 709-719.

Horak, M.; Palm, V.; Soogenbits, U. (1975). Kinetics of Grignard reagent formation. 2. Effect of the solvent and halide on organomagnesium compound formation. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(3), 721-733.

Juriaado, T.; Palm, V. (1975). Dissociation constants of substituted acetic acid derivatives and inductive conductivity of some alicyclic systems in aqueous methanol. Reaktsionnaya Sposobnost Organicheskikh Soedinenii , 12(1), 123-131.

Nummert, V.; Palm, V.; Uudam, M. (1975). Study of the possible applications of the atomic orbital energy model. 2. Determination of pKa values of formocholine and choline chlorides, and bis(diethylamino)methane. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 12(2), 445-456.

Palm, V. (1975). Study of the possible applications of the atomic orbital energy model. I. Modification of the orbital electronegativity concept and bond polarity model. Reaktsionnaya Sposobnost Organicheskikh Soedinenii , 12(2), 457-462.

Palm, V.; Linntam, A. (1975). Empirical dependence of orbital energies on nuclear charge and electronic configuration. The additivity of screening and nonscreening interactions between electrons. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 12(2), 463-474.

Nummert, V.; Palm, V. (1975). Kinetics of the alkaline hydrolysis of substituted phenyl p-toluene sulfonates. IX. Hydrolysis of o-carboxy-substituted phenyl p-toluene sulfonate. Quantitative interpretation of the salt effect using an electrostatic model. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(3), 581-601.

Palm, V.; Editor. (1975). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol.1(1). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 1(1)). 602 pp. Publisher: VINITI, Moscow, USSR.

Palm, V.; Editor. (1975). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol.1(2). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 1(2)). 299 pp. Publisher: VINITI, Moscow, USSR.

Koppel, I.; Karelson, M.; Palm, V. (1974). Common scale of inductive constants, s*, for neutral and charged substituents. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(1), 101-120.

Korgesaar, A.; Palm, V. (1974). Kinetics and mechanism of the reaction of hydrochloric acid with methanol, ethanol, and 1-propanol and conductometry of their respective solutions. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(1), 141-151.

Karelson, M.; Palm, V.; Hiob, R.; Haldna, U. (1974). Ionization mechanism of strong acids. Trichloroacetic, 2,4,6-trinitrobenzoic, and picric acids in aqueous sulfuric acid. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(1), 239-256.

Palm, V.; Karelson, M. (1974). New model for solutions of electrolytes. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(1), 263-268.

Talvik, I.; Palm, V. (1974). Attempt to interpret acidity of carbon acids using j-constants of substituents. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(2), 287-302.

Palm, V.; Korgesaar, A. (1974). Kinetic detection of conducting and nonconducting ion pairs in reactions of hydrogen chloride with methanol and ethanol. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(2), 523-537.

Karelson, M.; Haldna, U.; Palm, V. (1973). Common relation of the equivalent conductivity of complexes of a proton with oxonium bases and of the hydrated proton itself to their molecular size. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(1), 163-174.

Palm, V.; Nummert, V.; Pussa, T.; Karelson, M.; Koppel, I. (1973). Electrostatic contribution to polar effects of charged substituents and nature of primary salt effect. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(1), 223-242.

Palm, V.; Pussa, T.; Nummert, V.; Talvik, I. (1973). Kinetics of the hydrolysis of benzoates. IV. Polar effects of substituents in the alkyl part. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(1), 243-267.

Karelson, M.; Palm, V.; Haldna, U. (1973). Complexing of nitrosubstituted benzenes with proton in aqueous solutions of sulfuric acid studied by differential conductometry. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(1), 307-322.

Karelson, M.; Palm, V.; Haldna, U. (1973). Differential-conductometric study of the Hammett indicator 2,4-dinitroaniline. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(1), 323-331.

Palm, V.; Palm, N. (1973). Electrostatic model of intramolecular interactions. I. Basic principles and their application to formation enthalpies of alkanes, cyclohexane, and adamantane. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(2), 391-412.

Palm, V. (1973). Electrostatic model of intramolecular interactions. 2. Application to formation enthalpies of fluorine derivatives of methane, some oxygen-containing compounds, and methylamine. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(2), 413-428.

Koppel, I.; Karelson, M. M.; Palm, V. (1973). Demonstration of the universality of the constant a of inductive interaction. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(2), 497-514.

Istomin, B. I.; Palm, V. (1973). Application of the principle of polylinearity to standard thermodynamic characteristics of organic compounds. 8. Compounds with polyvalent functional groups such as -S-, -O-, -S(O),-n<,>NN,< and -00-(of bridging systems). Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(2), 537-565.

Istomin, B. I.; Palm, V. (1973). Application of the principle of polylinearity to standard thermodynamic characteristics of organic compounds. 9. Compounds with the polyvalent functional groups carbon-carbon triple and carbon-carbon and carbon–oxygen double bonds. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(2), 567-582.

Istomin, B. I.; Palm, V. (1973). Application of the principle of polylinearity to standard thermodynamic characteristics of organic compounds. 10. Formation enthalpies of polyfunctional derivatives of alkanes. Separation of the inductive term. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(2), 583-607.

Isotmin, B. I.; Palm, V.; Nummert, V. (1973). Kinetics of alkaline hydrolysis of m-and p- substituted phenyl acetates and ethyl benzoates. Reaktsionnaya Sposobnost Organicheskikh Soedinenii), 10(2), 609-616.

Istomin, B. I.; Palm, V. (1973). Application of the principle of polylinearity to standard thermodynamic characteristics of organic compounds. 11. One variant of a calculation diagram for polysubstituted derivatives of alkanes. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(4), 1005-1010.

Istomin, B. I.; Palm, V. (1973). Application of the principle of polylinearity to standard thermodynamic characteristics of organic compounds. 12. Separation of the resonance interaction term from the enthalpy of formation D Hf0. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(4), 1011-1024.

Istomin, B. I.; Palm, V. (1973). Application of the principle of polylinearity to standard thermodynamic characteristics of formation of RXj compounds. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(4), 1025-1028.

Palm, V.; Haldna, U.; Koppel, I. (1973). Acidity functions and solvation interactions. Reaktsionnaya Sposobnost Organicheskikh Soedineni, 10(4), 1029-1042.

Istomin, B. I.; Palm, V. (1972). Application of PPL [partial linearity principle] to standard thermodynamic characteristics of organic compounds. 2. Structural dependence of jRi constants on sets of constants joRi, jooRi, and FRi for alkyl substituents. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(2), 433-467.

Istomin, B. I.; Palm, V. (1972). Application of PPL to standard thermodynamic characteristics of organic compounds. 3. Enthalpies of formation of monosubstituted alkenes RiX with univalent saturated functional groups mercapto, amino, hydroxyl, chloro, bromo, iodo, and fluoro. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(2), 469-511.

Pussa, T.; Nummert, V.; Palm, V. (1972). Kinetics of hydrolysis of benzoates. I. Alkaline hydrolysis of substituted phenyl benzoates in water. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(3), 697-728.

Karelson, M.; Palm, V.; Haldna, U. (1972). Experimental proof of the constancy of hydrogen ion mobility in the sulfuric acid-water system and substantiation of the applicability of differential conductometric methods in studies of protolytic equilibriums. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(3), 831-846.

Istomin, B. I.; Palm, V. (1972). Application of PPL to standard thermodynamic characteristics of organic compounds. 4. Enthalpies of formation of monosubstituted alkanes RX with univalent functional groups CHO, COOH, CN, ONO2, NO2, CR = CH, C = CH, and C6H5. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(3), 847-870.

Pussa, T.; Nummert, V.; Palm, V. (1972). Kinetics of hydrolysis of benzoates. II. Alkaline hydrolysis of alkyl benzoates in water. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(3), 871-889.

Istomin, B. I.; Palm, V. (1972). Application of PPL to standard thermodynamic characteristics of organic compounds. 5. Contribution of hyperconjugative interaction between the alkyl groupand electron-deficient substituent to the enthalpy of the formation of RiX. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(4), 1089-1104.

Istomin, B. I.; Palm, V. (1972). Application of PPL to standard thermodynamic characteristics of organic compounds. 6. Analysis of the scheme for quantitative correlation with inductive and hyperconjugative contributions of standard formation enthalpies DH.deg.f(298.deg.K,g). Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(4), 1105-1128.

Pussa, T.; Palm, V. (1972). Kinetics of hydrolysis of benzoates. III. Acid hydrolysis of benzoates in water. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(4), 1209-1224.

Istomin, B. I.; Palm, V. (1972). Application of PPL to standard thermodynamic characteristics of organic compounds. 7. Isoparametric relation (Compensation effects) of thermodynamic functions for homologous series of compounds H(CH2)nX X = methyl, phenyl, vinyl, ethynyl, mercaptyl. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(4), 1225-1253.

Koppel, I.; Palm, V. (1972). Influence of the solvent on organic reactivity. Editor(s): Chapman, N. B. Advan. Linear Free Energy Relat. 203-280. Publisher: Plenum Publ. Co. Ltd., London, England.

Maremae, V.; Pussa, T.; Palm, V. (1971). Kinetics of alkaline hydrolysis of substituted phenyl p-toluenesulfonates. VI. Influence of ionic strength of the medium of hydrolysis rate of o-, m-, and p-N(CH3)3+-substituted phenyl p-toluenesulfonates. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 8(1), 127-151.

Koppel, I.; Palm, V. (1971). General equation for solvent effects. Reaktsionnaya Sposobnost Organicheskikh Soedinenii , 8(1), 291-301.

Talvik, I.; Palm, V. (1971). Additional values for steric substituent constants and check of the isostericity principle. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 8(2), 445-462.

Maremae, V.; Palm, V. (1971). Kinetics of alkaline hydrolysis of substituted phenyl p-toluenesulfonates. VII. Deviations from the Debye-Hueckel theory of the influence of ionic strength on alkaline hydrolysis rates for o-, m- and p-hydroxyphenyl p-toluenesulfonates in water. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 8(2), 591-618.

Aaviksaar, A.; Paris, J.; Palm, V. (1971). Relation between catalysis and binding in chymotrypsin reactions. Reaktsionnaya . Sposobnost Organicheskikh Soedinenii, 8(3), 817-832.

Istomin, B. I.; Palm, V. (1971). Thermochemical bond energies and mathematical equivalence of 1,3- and 1,4-schemes for nonbonded interactions in alkanes. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 8(3), 833-844.

Istomin, B. I.; Palm, V. (1971). Application of the partial linearity principle to standard thermodynamic characteristics of organic compounds. I. Equation for monosubstituted alkanes and testing its applicability to thiols and primary amines. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 8(3), 845-866.

Rodima, T. K.; Haldna, U.; Palm, V. (1971). Corrected values of the HM acidity function for aqueous sulfuric acid solutions. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 8(4), 1165-1187.

Rodima, T. K.; Haldna, U.; Palm, V. (1971), Physical meaning of the HMandHR acidity functions. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 8(4), 1189-1199.

Palm, V.; Lebedeva, N. D. (1970). Combination of the additivity principle with LFER for calculating enthalpies of formation of organic compounds. III. Accounting for conformational interactions in amines and substituted hydrazines and estimation of additive contributions of nitrogen-hydrogen, carbon-nitrogen, and nitrogen-nitrogen. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 7(2), 305-336.

Palm, V.; Juriaado, T. (1970). Unsuitability of the simple Broensted scheme for dissociation of trichloroacetic acid. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 7(2), 449-457.

Sikk, P.; Aaviksaar, A.; Godovikov, N. N.; Morozova, N. A.; Palm, V. (1970). Interaction of organophosphorus compounds with a-chymotrypsin. VI. Antichymotrypsin activity of O-ethyl-5-(w-ethylthioalkyl)-methylthiophosphonates and their methylsulfomethylates.Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 7(4), 986-1001.

Palm, V.; Lebedeva, N. D. (1969). Combination of the additivity principle with [linear free energy relationships] for calculation of enthalpies of formation of organic compounds. I. Specifying additives and calculation of conformational contributions for alkanes. Reaktsionnaya Sposobnost Organicheskikh Soedinenii 6(1), 61-83.

Lebedeva, N. D.; Palm, V.; Gutner, N. M. (1969). Combination of the additivity principle with LFER [linear free energy relationship] for calculation of enthalpies of formation of organic compounds. II. Correlation of inductive terms and estimation of the value of the universal constant of inductive interaction. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 6(1), 84-113.

Palm, V.; Istomin, B. I. (1969). Isoparametric relations. Generalization of isokinetic and analogous relations. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 6(2), 427-441.

Koppel, I.; Palm, V. (1969). Dependence of rate constants on the nature and composition of the solvent. XV. Quantitative empirical solvent polarity index on the basis of the formal theory of interaction. Reaktsionnaya Sposobnost Organicheskikh Soedineni, 6(2), 504-526.

Istomin, B. I.; Palm, V. (1969). Expediency of correlations using solvatochromic shifts. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 6(3), 710-719.

Palm, V. (1968). Absence of electrostatic interaction through the molecule frame. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 5(3), 583-600.

Haldna, U.; Palm, V. (1968). Using the additivity of pKa values for polysubstituted anilines during a study of the acidity of strongly-acid media. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 5(4), 965-977.

Haldna, U.; Kuura, H.; Tamme, M.; Palm, V. (1968). Kinetics of the bromination of 3-pentanone in aqueous sulfuric acid solutions. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 5(4), 1009-1032.

Aaviksaar, A.; Nolvak, I.; Palm, V. (1968). Mechanism of reactions of a-chymotrypsin with O-ethyl (p-nitrophenylethyl)phosphonate. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 5(4), 1053-1058.

Neimysheva, A.A.; Palm, V.A.; Semin, G.K.; Loshadkin, N.A.; Knunyants, I.L. (1967). Nucleophilic substitution in derivatives of phosphorus acids. 2. Relation between structure of phosphorus-containing compounds and reactivity – application of correlation equations. Journal of General Chemistry USSR, 37(10), 2140.

Palm, V. (1967). Principles of the Quantitative Theory of Organic Reactions. (Osnovy Kolichestvennoi Teorii Organicheskikh Reaktsii) 356 pp. Publisher: Khimiya, Leningrad.

Palm, V.; Neimysheva, A. A.; Knunyants, I. L. (1967). Correlation[of the neutral hydrolysis rates of dialkylphosphinic acid chlorides with the substituent constants. An unusual dependence[on the steric effects and hyperconjugation. Reaktsionnaya Sposobnost Organicheskikh Soedinenii), 4(1), 38-45.

Koppel, I.; Palm, V. (1967). Dependence of the activity coefficients and the rate constants on the nature and the composition of the solvent. XII. Relations between medium effects and the structure of the solvent molecules using the substituent constants. Reaktsionnaya Sposobnost Organicheskikh Soedineni, 4(2), 381-409.

Pyldoya, P. K.; Palm, V. (1967). The dependence of the ionization potentials of alkyl-substituted aliphatic derivatives on the induction constants and hyperconjugation. A new electronic effect of high intensity. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 4(4), 786-813.

Koppel, I.; Palm, V. (1967). Effect of the nature and composition of the solvent on rate constants. XIII. Use of the “dielectric” theory for calculating the effect of solvent on the solvolysis of tert-butyl chloride in individual (one-component) solvents. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 4(4), 862-891.

Koppel, I.; Palm, V. (1967). Effect of the nature and composition of the solvent on rate constants. XIV. Use of the “dielectric” approach for correlation of the effects of the medium on the solvolysis rate for tert-butyl chloride in binary solvents. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 4(4), 892-911.

Tamme, M.; Kuura, H.; Haldna, U.; Palm, V. (1967). Basicity of diethyl ketone. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 4(4), 912-919.

Palm, V.; Haldna, U.; Talvik, A. (1966). Basicity of carbonyl compounds. Chemistry of the Carbonyl Group, 421-460.

Talvik, I.; Palm, V. (1965). Kinetics and mechanism of the acid catalyzed hydrolysis of esters in water. II. Investigation of esters with electronegative groups in the acyl part. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 2(1), 110-121.

Aaviksaar, A.; Ilomets, T.; Palm, V. (1965). Kinetics and mechanism of enzymic catalysis. Influence of snake venoms on the hydrolysis rate of p-nitrophenyl acetate. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 2(1), 222-238.

Palm, V. (1965). Problem of the transmission of the inductive effect and of polar resonance through rings. Reaktsionnaya Sposobnost. Organicheskikh Soedinenii, 2(2), 123-134.

Haldna, U.; Kuura, H.; Erreline, L.; Palm, V. (1965). Kinetics of the bromination of acetone in aqueous solutions of sulfuric acid. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 2(2), 194-210.

Maremae, V.; Palm, V. (1965). Kinetics of the alkaline hydrolysis of substituted phenyl esters of toluenesulfonic acid. IV. Temperature dependence in the water solution. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 2(3), 209-227.

Palm, V. (1964). Dependence of the rate constants on the nature and the composition of solvent. I. General theory. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 1(1), 128-139.

Palm, V.; Korgesaar, A. (1964). Dependence of the rate constants on the nature and the composition of solvent. II. Application of the general theory in the case of the solvolysis of tertiary-BuCl in mixtures of alcs. with C6H6 and nitrobenzene and in mixts. of C6H6 and nitrobenzene. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 1(1), 140-169.

Koppel, I.; Palm, V. (1964). Dependence of the rate constants on the nature and the composition of solvent. III. Conductimetric investigation of the kinetics of very slow reactions. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 1(1), 170-183.

Maremae, V.; Palm, V. (1964). Kinetics of the alkaline hydrolysis of substituted phenyl esters of p-toluenesulfonic acid. I. Precise estimation of the induction constants s0. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 1(2), 85-102.

Koppel, I.; Korgessaar, A.; Palm, V. (1964). Dependence of the rate constants on the nature and composition of solvent. IV. Mechanism of solvolysis of tert-butyl chloride under electrophilic catalysis. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 1(2), 125-147.

Palm, V.; Korgesaar, A. (1964). Dependence of rate constants on the nature and composition of a solvent. VI. Reaction between HCl and aliphatic alcohols in alcohol-benzene and alcohol-nitrobenzene mixtures. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 1(2), 157-170.

Palm, V. (1963). Some practical problems of the use of correlation equations. Tr. Konf. po Probl. Primeneniya Korrelyatsion. Uravnenii v Organ. Khim., Tartusk. Gos. Univ., Tartu, 1962 ,Volume 2, 136-141.

Palm, V.A.; Vizgert, R.V. (1962). Correlation of rate constants in alkaline hydrolysis of aromatic sulfoacid esters, as dependent on structur of these compounds. Doklady Akademii Nauk SSSR, 142(5), 1091-1094.

Korgesaar, A.; Timotheus, V.; Palm, V. (1962). Dependence of the rate of reaction between alcohols and hydrochloric acid on the composition of the solvent. Tr. Konf. po Probl. Primeneniya Korrelyatsion. Uravnenii v Organ. Khim., Tartusk. Gos. Univ., Tartu, 265-282.

Palm, V.; Haldna, U.; Talvik, A.; Mei, A. (1962). Problems in connection with the protonation of carbonyl compounds and the mechanism of the acid hydrolysis of esters. Uch. Zap. Tartusk. Gos. Univ., No. 127, 91-96.

Palm, V.; Haldna, U.; Talvik, A.; Mei, A . (1962). Protonization of carbonyl compounds and the mechanism of acid hydrolysis of complex esters. Zhurnal Fizicheskoi Khimii , 36, 2499-2501.

Palm, V.A. (1961). Structure and reactivity of organic compounds (quantitative laws). Russian Chemical Reviews, 30(9), 471-498.

Kozlova, K.R.; Palm, V.A. (1961). Synthesis of tetraphenylboronsodium in a tetrahydrofuran solution. Zhurnal Obshchei Khimii, 31(9), 2922.

Haldna, U.; Palm, V. A. (1960). Reduction of basicities to a single standard state. Basicity of acetone. Doklady Akademii Nauk SSSR, 135, 667-670.

Talvik, A.J.; Palm, V.A. (1959). Reactive ability of anions of some carboxylic acids in the acid-catalysed enolization of acetone. Doklady Akademii Nauk SSSR, 129(6), 1349-1352.

Talvik, A.I.; Palm, V.A. (1959). Studies on the kinetics and mechanism of acid hydrolysis of ethyl acetate. Zhurnal Fizicheskoi Khimii, 33(6), 1214-1220.

Palm, V.; Palm, N.; Tenno, T. (2006). Computerized database and software for retrieval, processing and prognosis of rate and equilibrium constants of chemical reactions. Proceedings of the Estonian Academy of Sciences. Chemistry, 55(1), 3–13.

Palm, V.; Palm, N.; Tenno, T. (2004). Modification of data processing and interpretation of results related to the use of multiparameter correlation analysis: introduction of additional characteristics and criterias. Part 1. Application to the treatment of solvent effects. Journal of Physical Organic Chemistry, 17(10), 876– 889.

Palm, V.; Kiho, J.; Jalas, A.; Tenno, T.; Palm, N. (2004). Computerized Database on Chemical Reactivity (Rate and Equilibrium Constants) and Concerted Software for Retrieval, Processing, and Prognosis of Data. In: International Conference on Education and Information Systems: Technologies and Applications, vol. 2. Proceedings: International Conference on Education and Information Systems (EISTA ’04); Orlando, USA; 21-25 July, 2004. Orlando, USA: 2004, 190-195.

Palm, V.; Tenno, T.; Palm, N. (2004). Averaged Values and the Problem of Generality for Substituent Constants. In: The Tenth International Conference on Correlation Analysis in Chemistry (CAIC, X): The Tenth International Conference on Correlation Analysis in Chemistry; Busan, Korea; 2004.

Palm, N.; Palm, V. (2001). Verification of the Modified Approach to Solvation Effects on the Basis of Extended Data Set: III. Results of Statistical Data Treatment for Particular Processes. Russian Journal of Organic Chemistry, 37, 935-939.

Jalas, A.; Palm, V.; Tenno, T. (2001). A computerized storage and retrieval system of pKa values of hydrogen acids. Proceedings of the Estonian Academy of Sciences, Chemistry (2001), 50(3), 186-192.

Palm, V. (2001). Some fundamental criteria of the scientific method and the internal structure of science. R.Vihalemm (Editor.). Estonian studies in the history and philosophy of science (91-110). Dordrecht/Boston/London: Kluwer Academic Publishers.

Palm, V.; Jalas, A.; Tenno, T. (2001). pKa Database. Dissociation of Hydrogen Acids (http:/mega.chem.ut.ee/tktool/teadus/pkdb). 1.

Palm, N.; Palm, V. (2000). Verification of modified approach to solvation effects based on extended set of data series II: procedure and verification results of averaged statistical significance of solvent constants scales. Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii), 36(8), 1075-1104.

Palm, V.; Jalas, A.; Kiho, J.; Tenno, T. (1997). A computerized system for storage, processing and prognostication of data with orientation toward the use of correlation equations. Organic Reactivity (Tartu), 31(1), 111-133.

Jalas, A.; Kiho, J.; Palm, V.; Tenno, T. (1997). Data structure and menu-based access of the rate and equilibrium constants of heterolytic organic reactions database. Organic Reactivity (Tartu), 31(1), 135-140.

Palm, N.; Palm, V. (1997). Check of a modified approach to solvent effects by processing of an extended set of solvent-dependent data series. 1. Test of an earlier defined set of nine solvent parameters. Organic Reactivity (Tartu), 31(1), 141-158.

Palm, V.; Timotheus, V.; Pooga, H.; Kaasik, S.; Palm, N. (1996). Reinvestigation of the substituent, environmental, and temperature effects on the solvolysis kinetics of disubstituted Mannich bases of the general structure 3-X1C6H4NHCH2C(NO2)2C6H4X2-3. 1. The set of experimental data. Organic Reactivity (Tartu), 30(1), 69-72.

Palm, V.; Kaasik, S. (1996). Reinvestigation of the substituent, environmental, and temperature effects on the solvolysis kinetics of disubstituted Mannich bases of the general structure 3-X1C6H4NHCH2C(NO2)2C6H4X2-3. 2. Quantitative interpretation of combined substituent, solvent, and temperature effects. Organic Reactivity (Tartu), 30(1), 73-83.

Nummert, V.; Piirsalu, M.; Palm, V. (1996). Kinetic study of hydrolysis of benzoates. XIX. Influence of temperature on ortho effect for water solution. Isokinetic dependence in the case of additional ortho induction effect. Organic Reactivity (Tartu), 30(1), 85-94.

Palm, V. (1995). International Journal on Quantitative Structure-Reactivity and -Property Relations.[In: Org. React. (Tartu).,1995; 29(1)]. Palm, V.; Editor. Estonia, 121 pp. Publisher: (Tartu Univiversity, Tartu, Estonia).

Palm, V. (1995). Isosteric constants found by nonlinear procedure from Menshutkin reaction data. Organic Reactivity (Tartu), 29(1), 37-40.

Matveev, A. A.; Popov, A. F.; Palm, V. A.; Piskunova, Zh. P. (1993). Factors affecting rate of the Menshutkin reaction. 3. Temperature effect. Organic Reactivity (Tartu), 28(1), 35-38.

Nummert, V.; Palm, V. (1993). Kinetic study of alkaline hydrolysis of substituted phenyl tosylates. XX. Influence of temperature on ortho effect. Isokinetic dependence in the case of additional ortho inductive effect. Organic Reactivity (Tartu), 28(1), 63-71.

Nummert, V.; Piirsalu, M.; Palm, V. (1993). Kinetic study of alkaline hydrolysis of substituted phenyl tosylates. XXI. Influence of solvent on the ortho effect. Organic Reactivity (Tartu), 28(1), 82-87.

Leinbock, R.; Palm, V. (1993). Check of electrostatic model for structural effects on formation enthalpies and dipole moments. 1. Algorithm and computer program for calculations in the framework of model of atomic point charges. Organic Reactivity (Tartu), 28(1), 96-100.

Leinbock, R.; Palm, V. (1993). Check of electrostatic model for structural effects on formation enthalpies and dipole moments. 2. Results for alkanes and cycloalkanes, alkenes and alkynes. Organic Reactivity (Tartu), 28(1), 101-109.

Hiob, R.; Palm, V. (1993). Structural and temperature effects in the gas phase hydrogen abstraction reactions from compounds with general structure R-H. 1. Abstraction by hydrogen atom. Organic Reactivity (Tartu), 28(1), 110-118.

Hiob, R.; Palm, V. (1993). Structural and temperature effects in the gas phase hydrogen abstraction reactions from compounds with general structure R-H. 2. Abstraction by variable free radicals. Organic Reactivity (Tartu), 28(1), 119-124.

Palm, V.; Palm, N. (1993). On the total number and list of parameter scales significant for general quantitative description of solvent effects. Organic Reactivity (Tartu) 28(1), 125-150.

Nummert, V.; Piirsalu, M.; Palm, V. (1990). Kinetic study of alkaline hydrolysis of substituted phenyl tosylates. XVIII. Results of kinetic measurements of o-substituted tosylates in 80% aqueous dimethyl sulfoxide. Organic Reactivity (Tartu), 27(3-4), 99-127.

Palm, V. (1990). Computer-managed automatic data retrieval and prognosis system for rate and equilibrium constants of organic reactions. Journal of Chemical Information and Computer Science, 30(4), 409-412.

Palm, V. (Editor), (1990). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Suppl. Vol. 5, 690 pp. Tartu.

Palm, V. (Editor), (1990). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Suppl. Vol. 6, 869 pp. Tartu.

Palm, V. (Editor), (1989). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Suppl. Vol. 2, 714 pp. Tartu.

Palm, V. (Editor), (1989). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Suppl. Vol. 3, 794 pp. Tartu.

Palm, V. (Editor), (1989). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Suppl. Vol. 4, 623 pp. Tartu.

Tuulmets, A.; Horak, M.; Hansen, E.; Palm, V. (1987). Some structure-reactivity relationships for alkyl bromides in the Grignard reaction. Organic Reactivity (Tartu), 24(4), 412-424.

Palm, V.; Musaeva, M. F. (1986). An attempt at quantitative description of combined temperature and solvent effects for diene condensation. Organic Reactivity (Tartu), 23(1), 96-107.

Palm, V. A.; Hiob, R. J. (1986). Quantitative statistical interpretation of kinetic data in the gas phase homolysis. 8. Program for automatic computational estimation of rate constants of gas phase homolysis and heats of formation of covalent compounds. Organic Reactivity (Tartu), 23(4), 412-439.

Sild, V. A.; Palm, V. A.. (1986). Realization of the general algorithm of the solution of direct problems for homogeneous equilibrium-kinetic mechanistic schemes. Organic Reactivity (Tartu), 23(4), 482-506.

Koppel, I. A.; Molder, U. H.; Palm, V. A. (1985). Ab initio SCF LCAO MO calculations of molecules. IV. Proton affinities. Comparison with experiment. Organic Reactivity (Tartu), 22(1), 3-45.

Matveev, A. A.; Piskunova, Zh. P.; Palm, V. A.; Popov, A. F. (1985). Factors affecting rate of Menshutkin reaction. 1. Effect of amine structure. Organic Reactivity (Tartu), 22(1), 110-118.

Palm, N.; Palm, V. (1985). Determination of the kinetic-equilibrium parameters of the reaction of triphenylaluminum with benzophenone. Organic Reactivity (Tartu), 22(2), 131-141.

Popov, A. F.; Matveev, A. A.; Piskunova, Zh. P.; Palm, V. A. (1985). Factors affecting the rate of Menshutkin reaction. 2. Interdependence of reagent structure effects. Organic Reactivity (Tartu), 22(2), 153-161.

Nummert, V.; Eek, M.; Palm, V . (1985).Kinetic study of alkaline hydrolysis of substituted phenyl tosylates. XIV. Discussion of results of kinetic measurements in 80% aqueous dimethyl sulfoxide. Organic Reactivity (Tartu), 22(3), 263-294.

Palm, V. (Editor), (1985). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Suppl. Vol.1(3-5), 1276 pp. Tartu.

Palm, V. (Editor), (1984). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Suppl. Vol.1(1-2), 496 pp. Tartu.

Leinbok, R. A.; Palm, V. (1984). Nonlinear parametrization of equations for atomic spectral terms. 2. Data processing applying the minimization of relative standard deviation in the equation with a reduced number of parameters. Organic Reactivity (Tartu), 21(2), 127-143.

Juriado, T.; Palm, V. (1984). Program package for computer storage and automatic search of correlation equations and for calculation of rate and equilibrium constants. 1. Digital coding system of equations of chemical reactions. Organic Reactivity (Tartu), 21(3), 255-284.

Uri, A.; Tuulmets, A.; Palm, V. (1983). Transesterification of esters of carboxylic acids by titanium alcoholates. II. Transesterification of esters of aromatic acids. Organic Reactivity (Tartu), 20(1), 122-131.

Hiob, R.; Palm, V. (1983). Quantitative statistical interpretation of kinetic data in gas phase homolysis. 3. Calculation of conventional formation enthalpies of free radicals in the approximation of constant effective mean value of log A0 = 14.64. Organic Reactivity (Tartu), 20(2), 151-202.

Palm, V.; Hiob, R. (1983).Quantitative statistical interpretation of kinetic data in the gas phase homolysis. 4. Calculation of conventional formation enthalpies of free radicals based on experimental activation energies, isokinetic and isoentropic models. Organic Reactivity (Tartu), 20(2), 257-274.

Palm, V.; Hiob, R. (1983).Quantitative statistical interpretation of kinetic data in gas-phase homolysis. 5. Correlation of substituent effects on conventional formation enthalpies of substituted methyl radicals proceeding from isoentropic and isokinetic models. Organic Reactivity (Tartu), 20(2), 321-354.

Leinbok, R.; Palm, V. (1983). Nonlinear parametrization of equations for atomic spectral terms. 1. Specification of general character of dependence on orbital-orbital shielding constants. Organic Reactivity (Tartu), 20(3), 373-396.

Hiob, R.; Palm, V. (1983). Quantitative statistical interpretation of kinetic data in gas-phase homolysis. 6. Attempted simultaneous estimation of entropy and enthalpy contributions to free energy of activation. Organic Reactivity (Tartu), 20(3), 405-443.

Palm, V.; Hiob, R. (1982). Quantitative statistical interpretation of kinetic data in gas-phase homolysis. 2. Results of data treatment in the coordinates of the isokinetic relationship. Organic Reactivity (Tartu), 19(1), 120-140.

Palm, V.; Hiob, R. (1981). Structure effects in the kinetics of gas-phase homolysis. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, Tartu, 18(1), 149-168.

Palm, V.; Hiob, R. (1981). Quantitative statistical interpretation of kinetic data on gas-phase homolysis. 1. Refined computation scheme for heats of formation in the gas phase at 0°K. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, Tartu, 18(3), 445-484.

Nummert, V.; Palm, V. (1980). Study of solvent dependence of j°. 1. Statistical data handling. Organic Reactivity (Tartu), 17(3), 292-312.

Nummert, V.; Palm, V. (1980). Study of solvent dependence of r0. 2. Results and discussion. Organic Reactivity (Tartu), 17(3), 331-351.

Korgesaar, A.; Danilov, I.; Palm, V. (1979). Study of the reactivity of substituted bicyclo[2.2.2] octanes. 1. Formulation of the problem. Methods of synthesis of disubstituted derivatives of bicyclo[2.2.2]octane. Organic Reactivity (Tartu), 16(4), 521-528.

Palm, V. (1979). Interpretation of the primary kinetic salt effect. Probl. Khim. Kinet. , 162-179.

Palm, V.; Editor. (1979). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol. 5(2). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 5(2)). 283 pp. Publisher: VINITI, Moscow, USSR.

Karelson, M.; Palm, V. (1978). New model of electric conductivity of strong electrolyte solutions. Teoreticheskaya i Eksperimental’naya Khimiya, 14(6), 781-787.

Linntam, A. A.; Palm, V. A. (1978).The study of possible applications of atomic orbital energy model. 5. Statistical treatment of atomic spectral terms including electronic configurations up to 1s22s22p53d. Organic Reactivity (Tartu), 15(1), 93-123.

Palm, V.; Editor. (1978). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol. 5(1). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 5(1)). 656 pp. Publisher: VINITI, Moscow, USSR.

Riikoja, J.; Timotheus, H.; Palm, V. (1977). Check of experimental data on solvolysis kinetics of Mannich bases X1C6H4NHCH2C(NO2)2C6H4X2 used in parametrization of four-factor polylinear equation with all gross terms. Organic Reactivity (Tartu), 14(4), 507-526.

Palm, V. (1977). Principles of the Quantitative Theory of Organic Reactions. 2nd Ed. (Osnovy Kolichestvennoi Teorii Organicheskikh Reaktsii). 359 pp. Leningrad.

Palm, V.; Editor. (1977). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol. 2(2). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 2(2)). 618 pp. Publisher: VINITI, Moscow, USSR.

Palm, V.; Editor. (1977). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol. 3(1). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 3(1)). 463 pp. Publisher: VINITI, Moscow, USSR.

Palm, V.; Editor. (1977). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol. 3(2). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 3(2)). 591 pp. Publisher: VINITI, Moscow, USSR.

Palm, V.; Editor. (1977). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol. 4(1). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 4(1)). 580 pp. Publisher: VINITI, Moscow, USSR.

Palm, V.; Editor. (1977). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol. 4(2). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 4(2)). 432 pp. Publisher: VINITI, Moscow, USSR.

Palm, V.; Editor. (1976). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol. 2(1). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 2(1). 706 pp. Publisher: VINITI, Moscow, USSR.

Nummert, V.; Palm, V. (1976). Study of the electric conductivity of sodium o-tosyloxybenzoate in aqueous solutions of sodium hydroxide. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 13(1), 75-83.

Palm, V. (1976). Study of the possible applications of a model of atom orbital energies. 3. Evaluation of constants of paired shielding and nonshielding interactions of electrons for orbitals of the second shell. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 13(1), 117-130.

Palm, V. (1976). Study of the possible applications of a model of atom orbital energies. 4. Energetically accurate basis for quantum-chemical calculations and the possible procedure for the latter. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 13(1), 131-139.

Kozlov, V.; Ivanov, A.; Palm, V. (1976). On the ratio of meta and para isomers in equilibrium mixtures of disubstituted benzenes. Organic Reactivity (Tartu), 13(3), 315-327.

Karelson, M.; Palm, V. (1975). Hydrogen bond energy in ice I calculated using the method of electrostatic interactions between partial charges. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(3), 667-677.

Korgesaar, A.; Palm, V. (1975). Kinetics and mechanism of the reaction of hydrogen chloride with absolute aliphatic alcohols. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(3), 697-707.

Horak, M.; Palm, V.; Soogenbits, U. (1975). Kinetics of Grignard reagent formation. 1. Supplementary kinetic parameters and mechanism of the reaction. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(3), 709-719.

Horak, M.; Palm, V.; Soogenbits, U. (1975). Kinetics of Grignard reagent formation. 2. Effect of the solvent and halide on organomagnesium compound formation. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(3), 721-733.

Juriaado, T.; Palm, V. (1975). Dissociation constants of substituted acetic acid derivatives and inductive conductivity of some alicyclic systems in aqueous methanol. Reaktsionnaya Sposobnost Organicheskikh Soedinenii , 12(1), 123-131.

Nummert, V.; Palm, V.; Uudam, M. (1975). Study of the possible applications of the atomic orbital energy model. 2. Determination of pKa values of formocholine and choline chlorides, and bis(diethylamino)methane. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 12(2), 445-456.

Palm, V. (1975). Study of the possible applications of the atomic orbital energy model. I. Modification of the orbital electronegativity concept and bond polarity model. Reaktsionnaya Sposobnost Organicheskikh Soedinenii , 12(2), 457-462.

Palm, V.; Linntam, A. (1975). Empirical dependence of orbital energies on nuclear charge and electronic configuration. The additivity of screening and nonscreening interactions between electrons. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 12(2), 463-474.

Nummert, V.; Palm, V. (1975). Kinetics of the alkaline hydrolysis of substituted phenyl p-toluene sulfonates. IX. Hydrolysis of o-carboxy-substituted phenyl p-toluene sulfonate. Quantitative interpretation of the salt effect using an electrostatic model. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(3), 581-601.

Palm, V.; Editor. (1975). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol.1(1). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 1(1)). 602 pp. Publisher: VINITI, Moscow, USSR.

Palm, V.; Editor. (1975). Tables of Rate and Equilibrium Constants of Heterolytic Organic Reactions, Vol.1(2). (Tablitsy Konstant Skorosti i Ravnovesiya Geteroliticheskikh Organicheskikh Reaktsii, Tom 1(2)). 299 pp. Publisher: VINITI, Moscow, USSR.

Koppel, I.; Karelson, M.; Palm, V. (1974). Common scale of inductive constants, s*, for neutral and charged substituents. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(1), 101-120.

Korgesaar, A.; Palm, V. (1974). Kinetics and mechanism of the reaction of hydrochloric acid with methanol, ethanol, and 1-propanol and conductometry of their respective solutions. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(1), 141-151.

Karelson, M.; Palm, V.; Hiob, R.; Haldna, U. (1974). Ionization mechanism of strong acids. Trichloroacetic, 2,4,6-trinitrobenzoic, and picric acids in aqueous sulfuric acid. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(1), 239-256.

Palm, V.; Karelson, M. (1974). New model for solutions of electrolytes. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(1), 263-268.

Talvik, I.; Palm, V. (1974). Attempt to interpret acidity of carbon acids using j-constants of substituents. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(2), 287-302.

Palm, V.; Korgesaar, A. (1974). Kinetic detection of conducting and nonconducting ion pairs in reactions of hydrogen chloride with methanol and ethanol. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 11(2), 523-537.

Karelson, M.; Haldna, U.; Palm, V. (1973). Common relation of the equivalent conductivity of complexes of a proton with oxonium bases and of the hydrated proton itself to their molecular size. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(1), 163-174.

Palm, V.; Nummert, V.; Pussa, T.; Karelson, M.; Koppel, I. (1973). Electrostatic contribution to polar effects of charged substituents and nature of primary salt effect. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(1), 223-242.

Palm, V.; Pussa, T.; Nummert, V.; Talvik, I. (1973). Kinetics of the hydrolysis of benzoates. IV. Polar effects of substituents in the alkyl part. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(1), 243-267.

Karelson, M.; Palm, V.; Haldna, U. (1973). Complexing of nitrosubstituted benzenes with proton in aqueous solutions of sulfuric acid studied by differential conductometry. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(1), 307-322.

Karelson, M.; Palm, V.; Haldna, U. (1973). Differential-conductometric study of the Hammett indicator 2,4-dinitroaniline. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(1), 323-331.

Palm, V.; Palm, N. (1973). Electrostatic model of intramolecular interactions. I. Basic principles and their application to formation enthalpies of alkanes, cyclohexane, and adamantane. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(2), 391-412.

Palm, V. (1973). Electrostatic model of intramolecular interactions. 2. Application to formation enthalpies of fluorine derivatives of methane, some oxygen-containing compounds, and methylamine. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(2), 413-428.

Koppel, I.; Karelson, M. M.; Palm, V. (1973). Demonstration of the universality of the constant a of inductive interaction. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(2), 497-514.

Istomin, B. I.; Palm, V. (1973). Application of the principle of polylinearity to standard thermodynamic characteristics of organic compounds. 8. Compounds with polyvalent functional groups such as -S-, -O-, -S(O),-n<,>NN,< and -00-(of bridging systems). Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(2), 537-565.

Istomin, B. I.; Palm, V. (1973). Application of the principle of polylinearity to standard thermodynamic characteristics of organic compounds. 9. Compounds with the polyvalent functional groups carbon-carbon triple and carbon-carbon and carbon–oxygen double bonds. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(2), 567-582.

Istomin, B. I.; Palm, V. (1973). Application of the principle of polylinearity to standard thermodynamic characteristics of organic compounds. 10. Formation enthalpies of polyfunctional derivatives of alkanes. Separation of the inductive term. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(2), 583-607.

Isotmin, B. I.; Palm, V.; Nummert, V. (1973). Kinetics of alkaline hydrolysis of m-and p- substituted phenyl acetates and ethyl benzoates. Reaktsionnaya Sposobnost Organicheskikh Soedinenii), 10(2), 609-616.

Istomin, B. I.; Palm, V. (1973). Application of the principle of polylinearity to standard thermodynamic characteristics of organic compounds. 11. One variant of a calculation diagram for polysubstituted derivatives of alkanes. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(4), 1005-1010.

Istomin, B. I.; Palm, V. (1973). Application of the principle of polylinearity to standard thermodynamic characteristics of organic compounds. 12. Separation of the resonance interaction term from the enthalpy of formation D Hf0. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(4), 1011-1024.

Istomin, B. I.; Palm, V. (1973). Application of the principle of polylinearity to standard thermodynamic characteristics of formation of RXj compounds. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 10(4), 1025-1028.

Palm, V.; Haldna, U.; Koppel, I. (1973). Acidity functions and solvation interactions. Reaktsionnaya Sposobnost Organicheskikh Soedineni, 10(4), 1029-1042.

Istomin, B. I.; Palm, V. (1972). Application of PPL [partial linearity principle] to standard thermodynamic characteristics of organic compounds. 2. Structural dependence of jRi constants on sets of constants joRi, jooRi, and FRi for alkyl substituents. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(2), 433-467.

Istomin, B. I.; Palm, V. (1972). Application of PPL to standard thermodynamic characteristics of organic compounds. 3. Enthalpies of formation of monosubstituted alkenes RiX with univalent saturated functional groups mercapto, amino, hydroxyl, chloro, bromo, iodo, and fluoro. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(2), 469-511.

Pussa, T.; Nummert, V.; Palm, V. (1972). Kinetics of hydrolysis of benzoates. I. Alkaline hydrolysis of substituted phenyl benzoates in water. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(3), 697-728.

Karelson, M.; Palm, V.; Haldna, U. (1972). Experimental proof of the constancy of hydrogen ion mobility in the sulfuric acid-water system and substantiation of the applicability of differential conductometric methods in studies of protolytic equilibriums. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(3), 831-846.

Istomin, B. I.; Palm, V. (1972). Application of PPL to standard thermodynamic characteristics of organic compounds. 4. Enthalpies of formation of monosubstituted alkanes RX with univalent functional groups CHO, COOH, CN, ONO2, NO2, CR = CH, C = CH, and C6H5. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(3), 847-870.

Pussa, T.; Nummert, V.; Palm, V. (1972). Kinetics of hydrolysis of benzoates. II. Alkaline hydrolysis of alkyl benzoates in water. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(3), 871-889.

Istomin, B. I.; Palm, V. (1972). Application of PPL to standard thermodynamic characteristics of organic compounds. 5. Contribution of hyperconjugative interaction between the alkyl groupand electron-deficient substituent to the enthalpy of the formation of RiX. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(4), 1089-1104.

Istomin, B. I.; Palm, V. (1972). Application of PPL to standard thermodynamic characteristics of organic compounds. 6. Analysis of the scheme for quantitative correlation with inductive and hyperconjugative contributions of standard formation enthalpies DH.deg.f(298.deg.K,g). Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(4), 1105-1128.

Pussa, T.; Palm, V. (1972). Kinetics of hydrolysis of benzoates. III. Acid hydrolysis of benzoates in water. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(4), 1209-1224.

Istomin, B. I.; Palm, V. (1972). Application of PPL to standard thermodynamic characteristics of organic compounds. 7. Isoparametric relation (Compensation effects) of thermodynamic functions for homologous series of compounds H(CH2)nX X = methyl, phenyl, vinyl, ethynyl, mercaptyl. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 9(4), 1225-1253.

Koppel, I.; Palm, V. (1972). Influence of the solvent on organic reactivity. Editor(s): Chapman, N. B. Advan. Linear Free Energy Relat. 203-280. Publisher: Plenum Publ. Co. Ltd., London, England.

Maremae, V.; Pussa, T.; Palm, V. (1971). Kinetics of alkaline hydrolysis of substituted phenyl p-toluenesulfonates. VI. Influence of ionic strength of the medium of hydrolysis rate of o-, m-, and p-N(CH3)3+-substituted phenyl p-toluenesulfonates. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 8(1), 127-151.

Koppel, I.; Palm, V. (1971). General equation for solvent effects. Reaktsionnaya Sposobnost Organicheskikh Soedinenii , 8(1), 291-301.

Talvik, I.; Palm, V. (1971). Additional values for steric substituent constants and check of the isostericity principle. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 8(2), 445-462.

Maremae, V.; Palm, V. (1971). Kinetics of alkaline hydrolysis of substituted phenyl p-toluenesulfonates. VII. Deviations from the Debye-Hueckel theory of the influence of ionic strength on alkaline hydrolysis rates for o-, m- and p-hydroxyphenyl p-toluenesulfonates in water. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 8(2), 591-618.

Aaviksaar, A.; Paris, J.; Palm, V. (1971). Relation between catalysis and binding in chymotrypsin reactions. Reaktsionnaya . Sposobnost Organicheskikh Soedinenii, 8(3), 817-832.

Istomin, B. I.; Palm, V. (1971). Thermochemical bond energies and mathematical equivalence of 1,3- and 1,4-schemes for nonbonded interactions in alkanes. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 8(3), 833-844.

Istomin, B. I.; Palm, V. (1971). Application of the partial linearity principle to standard thermodynamic characteristics of organic compounds. I. Equation for monosubstituted alkanes and testing its applicability to thiols and primary amines. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 8(3), 845-866.

Rodima, T. K.; Haldna, U.; Palm, V. (1971). Corrected values of the HM acidity function for aqueous sulfuric acid solutions. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 8(4), 1165-1187.

Rodima, T. K.; Haldna, U.; Palm, V. (1971), Physical meaning of the HMandHR acidity functions. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 8(4), 1189-1199.

Palm, V.; Lebedeva, N. D. (1970). Combination of the additivity principle with LFER for calculating enthalpies of formation of organic compounds. III. Accounting for conformational interactions in amines and substituted hydrazines and estimation of additive contributions of nitrogen-hydrogen, carbon-nitrogen, and nitrogen-nitrogen. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 7(2), 305-336.

Palm, V.; Juriaado, T. (1970). Unsuitability of the simple Broensted scheme for dissociation of trichloroacetic acid. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 7(2), 449-457.

Sikk, P.; Aaviksaar, A.; Godovikov, N. N.; Morozova, N. A.; Palm, V. (1970). Interaction of organophosphorus compounds with a-chymotrypsin. VI. Antichymotrypsin activity of O-ethyl-5-(w-ethylthioalkyl)-methylthiophosphonates and their methylsulfomethylates.Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 7(4), 986-1001.

Palm, V.; Lebedeva, N. D. (1969). Combination of the additivity principle with [linear free energy relationships] for calculation of enthalpies of formation of organic compounds. I. Specifying additives and calculation of conformational contributions for alkanes. Reaktsionnaya Sposobnost Organicheskikh Soedinenii 6(1), 61-83.

Lebedeva, N. D.; Palm, V.; Gutner, N. M. (1969). Combination of the additivity principle with LFER [linear free energy relationship] for calculation of enthalpies of formation of organic compounds. II. Correlation of inductive terms and estimation of the value of the universal constant of inductive interaction. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 6(1), 84-113.

Palm, V.; Istomin, B. I. (1969). Isoparametric relations. Generalization of isokinetic and analogous relations. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 6(2), 427-441.

Koppel, I.; Palm, V. (1969). Dependence of rate constants on the nature and composition of the solvent. XV. Quantitative empirical solvent polarity index on the basis of the formal theory of interaction. Reaktsionnaya Sposobnost Organicheskikh Soedineni, 6(2), 504-526.

Istomin, B. I.; Palm, V. (1969). Expediency of correlations using solvatochromic shifts. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 6(3), 710-719.

Palm, V. (1968). Absence of electrostatic interaction through the molecule frame. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 5(3), 583-600.

Haldna, U.; Palm, V. (1968). Using the additivity of pKa values for polysubstituted anilines during a study of the acidity of strongly-acid media. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 5(4), 965-977.

Haldna, U.; Kuura, H.; Tamme, M.; Palm, V. (1968). Kinetics of the bromination of 3-pentanone in aqueous sulfuric acid solutions. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 5(4), 1009-1032.

Aaviksaar, A.; Nolvak, I.; Palm, V. (1968). Mechanism of reactions of a-chymotrypsin with O-ethyl (p-nitrophenylethyl)phosphonate. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 5(4), 1053-1058.

Neimysheva, A.A.; Palm, V.A.; Semin, G.K.; Loshadkin, N.A.; Knunyants, I.L. (1967). Nucleophilic substitution in derivatives of phosphorus acids. 2. Relation between structure of phosphorus-containing compounds and reactivity – application of correlation equations. Journal of General Chemistry USSR, 37(10), 2140.

Palm, V. (1967). Principles of the Quantitative Theory of Organic Reactions. (Osnovy Kolichestvennoi Teorii Organicheskikh Reaktsii) 356 pp. Publisher: Khimiya, Leningrad.

Palm, V.; Neimysheva, A. A.; Knunyants, I. L. (1967). Correlation[of the neutral hydrolysis rates of dialkylphosphinic acid chlorides with the substituent constants. An unusual dependence[on the steric effects and hyperconjugation. Reaktsionnaya Sposobnost Organicheskikh Soedinenii), 4(1), 38-45.

Koppel, I.; Palm, V. (1967). Dependence of the activity coefficients and the rate constants on the nature and the composition of the solvent. XII. Relations between medium effects and the structure of the solvent molecules using the substituent constants. Reaktsionnaya Sposobnost Organicheskikh Soedineni, 4(2), 381-409.

Pyldoya, P. K.; Palm, V. (1967). The dependence of the ionization potentials of alkyl-substituted aliphatic derivatives on the induction constants and hyperconjugation. A new electronic effect of high intensity. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 4(4), 786-813.

Koppel, I.; Palm, V. (1967). Effect of the nature and composition of the solvent on rate constants. XIII. Use of the “dielectric” theory for calculating the effect of solvent on the solvolysis of tert-butyl chloride in individual (one-component) solvents. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 4(4), 862-891.

Koppel, I.; Palm, V. (1967). Effect of the nature and composition of the solvent on rate constants. XIV. Use of the “dielectric” approach for correlation of the effects of the medium on the solvolysis rate for tert-butyl chloride in binary solvents. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 4(4), 892-911.

Tamme, M.; Kuura, H.; Haldna, U.; Palm, V. (1967). Basicity of diethyl ketone. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 4(4), 912-919.

Palm, V.; Haldna, U.; Talvik, A. (1966). Basicity of carbonyl compounds. Chemistry of the Carbonyl Group, 421-460.

Talvik, I.; Palm, V. (1965). Kinetics and mechanism of the acid catalyzed hydrolysis of esters in water. II. Investigation of esters with electronegative groups in the acyl part. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 2(1), 110-121.

Aaviksaar, A.; Ilomets, T.; Palm, V. (1965). Kinetics and mechanism of enzymic catalysis. Influence of snake venoms on the hydrolysis rate of p-nitrophenyl acetate. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 2(1), 222-238.

Palm, V. (1965). Problem of the transmission of the inductive effect and of polar resonance through rings. Reaktsionnaya Sposobnost. Organicheskikh Soedinenii, 2(2), 123-134.

Haldna, U.; Kuura, H.; Erreline, L.; Palm, V. (1965). Kinetics of the bromination of acetone in aqueous solutions of sulfuric acid. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 2(2), 194-210.

Maremae, V.; Palm, V. (1965). Kinetics of the alkaline hydrolysis of substituted phenyl esters of toluenesulfonic acid. IV. Temperature dependence in the water solution. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 2(3), 209-227.

Palm, V. (1964). Dependence of the rate constants on the nature and the composition of solvent. I. General theory. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 1(1), 128-139.

Palm, V.; Korgesaar, A. (1964). Dependence of the rate constants on the nature and the composition of solvent. II. Application of the general theory in the case of the solvolysis of tertiary-BuCl in mixtures of alcs. with C6H6 and nitrobenzene and in mixts. of C6H6 and nitrobenzene. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 1(1), 140-169.

Koppel, I.; Palm, V. (1964). Dependence of the rate constants on the nature and the composition of solvent. III. Conductimetric investigation of the kinetics of very slow reactions. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 1(1), 170-183.

Maremae, V.; Palm, V. (1964). Kinetics of the alkaline hydrolysis of substituted phenyl esters of p-toluenesulfonic acid. I. Precise estimation of the induction constants s0. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 1(2), 85-102.

Koppel, I.; Korgessaar, A.; Palm, V. (1964). Dependence of the rate constants on the nature and composition of solvent. IV. Mechanism of solvolysis of tert-butyl chloride under electrophilic catalysis. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 1(2), 125-147.

Palm, V.; Korgesaar, A. (1964). Dependence of rate constants on the nature and composition of a solvent. VI. Reaction between HCl and aliphatic alcohols in alcohol-benzene and alcohol-nitrobenzene mixtures. Reaktsionnaya Sposobnost Organicheskikh Soedinenii, 1(2), 157-170.

Palm, V. (1963). Some practical problems of the use of correlation equations. Tr. Konf. po Probl. Primeneniya Korrelyatsion. Uravnenii v Organ. Khim., Tartusk. Gos. Univ., Tartu, 1962 ,Volume 2, 136-141.

Palm, V.A.; Vizgert, R.V. (1962). Correlation of rate constants in alkaline hydrolysis of aromatic sulfoacid esters, as dependent on structur of these compounds. Doklady Akademii Nauk SSSR, 142(5), 1091-1094.

Korgesaar, A.; Timotheus, V.; Palm, V. (1962). Dependence of the rate of reaction between alcohols and hydrochloric acid on the composition of the solvent. Tr. Konf. po Probl. Primeneniya Korrelyatsion. Uravnenii v Organ. Khim., Tartusk. Gos. Univ., Tartu, 265-282.

Palm, V.; Haldna, U.; Talvik, A.; Mei, A. (1962). Problems in connection with the protonation of carbonyl compounds and the mechanism of the acid hydrolysis of esters. Uch. Zap. Tartusk. Gos. Univ., No. 127, 91-96.

Palm, V.; Haldna, U.; Talvik, A.; Mei, A . (1962). Protonization of carbonyl compounds and the mechanism of acid hydrolysis of complex esters. Zhurnal Fizicheskoi Khimii , 36, 2499-2501.

Palm, V.A. (1961). Structure and reactivity of organic compounds (quantitative laws). Russian Chemical Reviews, 30(9), 471-498.

Kozlova, K.R.; Palm, V.A. (1961). Synthesis of tetraphenylboronsodium in a tetrahydrofuran solution. Zhurnal Obshchei Khimii, 31(9), 2922.

Haldna, U.; Palm, V. A. (1960). Reduction of basicities to a single standard state. Basicity of acetone. Doklady Akademii Nauk SSSR, 135, 667-670.

Talvik, A.J.; Palm, V.A. (1959). Reactive ability of anions of some carboxylic acids in the acid-catalysed enolization of acetone. Doklady Akademii Nauk SSSR, 129(6), 1349-1352.

Talvik, A.I.; Palm, V.A. (1959). Studies on the kinetics and mechanism of acid hydrolysis of ethyl acetate. Zhurnal Fizicheskoi Khimii, 33(6), 1214-1220.