Quantitative Models of Steric Effects

[1]  Einar J. Salmi.  Untersuchungen über ätherartige Verbindungen, VI. Mitteil.: Zur Kenntnis der konstitutiven Faktoren bei der sauren Hydrolyse der Ester aliphatischer Carbonsäuren† , 1939 .

[2]  Hilton A. Smith,et al.  The Acid Catalyzed Esterification of Normal Fatty Acids , 1941 .

[3]  M. Charton,et al.  Nature of the ortho effect. II. Composition of the Taft steric parameters , 1969 .

[4]  B. Karger,et al.  Foam Fractionation under Total Reflux. Recovery and Concentration of Ionic Species from Aqueous Solution. , 1966 .

[5]  Edward A. Meyers,et al.  Quantitative Separation of Hyperconjugation Effects from Steric Substituent Constants , 1961 .

[6]  S H Unger,et al.  "Aromatic" substituent constants for structure-activity correlations. , 1973, Journal of medicinal chemistry.

[7]  W. Todd Wipke,et al.  Congestion. Conformation-dependent measure of steric environment. Derivation and application in stereoselective addition to unsaturated carbon , 1974 .

[8]  L. Snyder.  Linear elution adsorption chromatography , 1961 .

[9]  T. Fujita,et al.  Nature and composition of Taft-Hancock steric constants , 1973 .

[10]  C. Hansch,et al.  The use of homolytic, steric, and hydrophobic constants in a structure-activity study of 1,3-benzodioxole synergists. , 1968, Journal of medicinal chemistry.

[11]  K. Kindler.  Ortho-Effekt und Reaktionsfähigkeit. I. Über Größe und Ursachen des Ortho-Effektes bei der hydrolyse aromatischer Ester , 1928 .

[12]  H. Eyring.  STERIC HINDRANCE AND COLLISION DIAMETERS1 , 1932 .

[13]  F. Kehrmann.  Zur Entdeckungsgeschichte der Regeln der sogenannten »sterischen Hinderungen« und zur Wahrung meiner Priorität , 1908 .

[14]  K. Bowden,et al.  Structure-activity relations. 3. Bronchodilator activity of substituted 6-thioxanthines. , 1973, Biochemical pharmacology.

[15]  Joseph S. Wall,et al.  Relative Nucleophilic Reactivities of Amino Groups and Mercaptide Ions in Addition Reactions with α,β-Unsaturated Compounds1,2 , 1965 .

[16]  Robert W. Taft,et al.  Linear Steric Energy Relationships , 1953 .

[17]  C. Hancock,et al.  Equilibrium and Kinetic Studies of the Meerwein-Ponndorf-Verley-Oppenauer (MPVO) Reaction1 , 1965 .

[18]  E. Berliner.  Some thoughts on the baker-nathan order☆☆☆ , 1959 .

[19]  R. Taft,et al.  The Evaluation of Inductive and Steric Effects on Reactivity. The Methoxide Ioncatalyzed Rates of Methanolysis of l-Menthyl Esters in Methanol1 , 1957 .

[20]  C. Hansch,et al.  Steric parameters in drug design. Monoamine oxidase inhibitors and antihistamines. , 1969, Journal of medicinal chemistry.

[21]  F. Kehrmann.  Untersuchungen über den Einfluss von Natur und Stellung gewisser Atome und Atomgruppen im Benzolkern auf die Ersetzbarkeit des Chinon‐Sauerstoffs durch die Isonitroso‐Gruppe , 1889 .

[22]  D. Rorabacher,et al.  Steric effects of chelation kinetics. III. Reactions of aquonickel(II) ion with N-alkyl-substituted ethylenediamines , 1972 .

[23]  R. Taft,et al.  The Evaluation of Inductive and Resonance Effects on Reactivity. I. Hydrolysis Rates of Acetals of Non-conjugated Aldehydes and Ketones1a , 1955 .

[24]  E. A. Moelwyn-Hughes.  IX. The kinetics of chemical change in solution , 1932 .

[25]  J. J. Sudborough,et al.  XLV.—Etherification constants of substituted acetic acids , 2022 .

[26]  C. Hancock,et al.  Correlations between Structure and Nuclear Magnetic Resonance Spectra for Aliphatic Esters1 , 1966 .

[27]  V. Meyer.  Ueber ein seltsames Gesetz bei der Esterbildung aromatischer Säuren , 1894 .

[28]  H. Levenson,et al.  The Saponification of Ethyl Esters of Aliphatic Acids , 1940 .

[29]  N. Menschutkin.  Ueber den Einflufs der Isomerie der Alkohole und der Säuren auf die Bildung zusammengesetzter Aether , 1879 .

[30]  A. Michael.  Über die Beziehung zwischen Struktur der Fettalkohole und Geschwindigkeit der Esterifikation , 1909 .

[31]  R. Taft,et al.  Evaluation of resonance effects on reactivity by application of the linear inductive energy relationship-IV: Hyperconjugation effects of para-alkyl groups , 1959 .

[32]  T. R. Fukuto.  Physico-organic chemical approach to the mode of action of organophosphorus insecticides. , 1969, Residue reviews.

[33]  G. Vernin.  Les applications de la théorie de la chromatographie d'adsorption lineaire de Snyder en série hétérocyclique , 1970 .

[34]  Hilton A. Smith,et al.  Kinetics of the Catalyzed Esterification of Normal Aliphatic Acids in Methyl Alcohol , 1939 .

[35]  Zeno Simon,et al.  Specific Interactions. Intermolecular Forces, Steric Requirements, and Molecular Size , 1974 .

[36]  A. Skrabal.  Reaktionsgeschwindigkeit-Temperatur-Studien , 1916 .

[37]  K. Schaffner,et al.  Protonenresonanzspektroskopische Untersuchungen an Bicyclo [2.2.1]heptan‐ und Bicyclo[2.2.2]octan‐Derivaten: Einfluss von Substituenten auf die chemische Verschiebung , 1967 .

[38]  C. Hansch,et al.  An analysis of the structure-activity relationship in the adrenergic blocking activity of the beta-haloalkylamines. , 1968, Biochemical pharmacology.

[39]  H. B. Klevens,et al.  Geometry and Spectra of Substituted Anilines , 1949 .

[40]  C. Hansch,et al.  The use of substituent constants in the quantitative treatment of hapten-antibody interaction. , 1969, Archives of biochemistry and biophysics.

[41]  K. Bowden,et al.  The reduction of substituted acetophenones by sodium borohydride , 1966 .

[42]  F. Kehrmann.  Ueber die Abhängigkeit der Substitutionsvorgänge von der Atom‐ und Moleculargrösse der Substituenten , 1890 .

[43]  W. M. Schubert,et al.  Electron donor and acceptor properties of alkyl substituents , 1962 .

[44]  A Hammett-Taft Polar-Steric Equation for the Saponification Rates of m- and p-Substituted Alkyl Benzoates1 , 1961 .

[45]  C. Hansch,et al.  THE USE OF SUBSTITUENT CONSTANTS AND REGRESSION ANALYSIS IN THE STUDY OF ENZYMATIC REACTION MECHANISMS. , 1965, Journal of the American Chemical Society.

[46]  S. V. Anantakrishnan,et al.  Kinetic studies in ester hydrolysis , 1941 .

[47]  R. Turner.  The thermochemical evidence for hyperconjugation , 1959 .

[48]  J. Topliss,et al.  Chance correlations in structure-activity studies using multiple regression analysis , 1972 .

[49]  H. Zollinger,et al.  Stereochemistry of the σ-Complex Intermediate in Sterically Hindered Electrophilic Aromatic Substitutions. (20th communication on diazo coupling reactions)† , 1970 .

[50]  S. Nozakura,et al.  Argentation Constants of Styrene Derivatives , 1969 .

[51]  Hilton A. Smith,et al.  Kinetics of the Esterification of Cyclohexanoic Acid and of the Saponification of its Ethyl Ester , 1940 .

[52]  C. Hancock,et al.  Alkaline hydrolysis and nuclear magnetic resonance spectra of some thiol esters , 1973 .

[53]  V. Meyer.  Ueber die Esterbildung aromatischer Säuren , 1895 .

[54]  J. Katzhendler,et al.  Organic Carbonates. Part XIII. Separation of Polar and Steric Effects in the Hydrolyses of Substituted Ethylene and Trimethylene Carbonates , 1972 .

[55]  Stefan H. Unger,et al.  Model building in structure-activity relations. Reexamination of adrenergic blocking activity of .beta.-halo-.beta.-arylalkylamines , 1973 .

[56]  A. Leo,et al.  Partition coefficients and their uses , 1971 .

[57]  A. K. Willard,et al.  Carbon-13-hydrogen coupling constants of hindered molecules. Possible measure of sterically induced rehybridization , 1970 .

[58]  P. N. Craig,et al.  Structure-activity correlations of antimalarial compounds. 2. Phenanthreneaminoalkylcarbinol antimalarials. , 1973, Journal of medicinal chemistry.

[59]  J. Halpern,et al.  Reactions of bis(dioximato)cobalt(II) complexes with organic halides. Influence of electronic and steric factors upon re-activity , 1972 .

[60]  G. Lamaty,et al.  Reactions d'addition nucléophile sur les cétones , 1971 .

[61]  G. T. Davis,et al.  Fluorine Nuclear Magnetic Resonance Shielding in p-Substituted Fluorobenzenes. The Influence of Structure and Solvent on Resonance Effects , 1963 .

[62]  Corwin Hansch,et al.  α-Chymotrypsin: A Case Study of Substituent Constants and Regression Analysis in Enzymic Structure—Activity Relationships , 1970 .

[63]  M. Newman,et al.  Synthesis and Properties of Highly Hindered Aliphatic Acids , 1963 .

[64]  D. Rorabacher,et al.  Steric effects on the kinetics and equilibriums of nickel(II)-alkylamine reactions in aqueous solution , 1971 .

[65]  R. Wegscheider.  Ueber die Esterbildung , 1895 .

[66]  Hilton A. Smith,et al.  Kinetics of the Saponification of the Ethyl Esters of Normal Aliphatic Acids , 1939 .

[67]  Robert W. Taft,et al.  Polar and Steric Substituent Constants for Aliphatic and o-Benzoate Groups from Rates of Esterification and Hydrolysis of Esters1 , 1952 .

[68]  W. Hückel.  Molekülbau und Reaktionsgeschwindigkeit , 1934 .

[69]  T. L. Hill,et al.  Steric Effects. I. Van der Waals Potential Energy Curves , 1948 .

[70]  M. Newman.  Some Observations Concerning Steric Factors , 1950 .

[71]  J. W. Baker.  Substituent effects on hyperconjugation: Evaluation of hyperconjugation energy for groups of the type ·CH2X , 1959 .

[72]  M. Charton,et al.  Definition of “Inductive” Substituent Constants , 1964 .

[73]  C. Hansch.  Quantitative approach to biochemical structure-activity relationships , 1969 .

[74]  V. Stella,et al.  Kinetics of the acid-catalyzed closure of hydantoic acids. Effect of 2-aryl and 2-alkyl substituents , 1973 .

[75]  V. J. Shiner.  Deuterium isotope effects and hyperconjugation , 1959 .

[76]  C. Hancock,et al.  The Change in the Six Number as a Variable in Quantitative Structure-Reactivity Correlations of Esters , 1963 .

[77]  R. Carter,et al.  Experiments on the Nature of Steric Isotope Effects , 1973 .

[78]  J. Steele,et al.  The Acid Catalyzed Hydrolysis of Ethyl Esters of Aliphatic Acids , 1941 .