Search Results - "Le Noble, W. J"

Activation and Reaction Volumes in Solution. 3 by Drljaca, A, Hubbard, C. D, van Eldik, R, Asano, T, Basilevsky, M. V, le Noble, W. J

“…A review of the literature of activation and reaction volumes of chemical reactions in solution is presented…”
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Activation and reaction volumes in solution. 2 by Van Eldik, R, Asano, T, Le Noble, W. J

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Hyperconjugation as a stereoinductive factor in the approach of electrophiles to trigonal carbon by Srivastava, S, Le Noble, W. J

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Activation and reaction volumes in solution by Asano, T, Le Noble, W. J

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Temperature and Para-Substituent Effects on the Face Selectivity of 1,3-Dipolar Cycloaddition Reactions of Benzonitrile Oxides with 5-Substituted Adamantane-2-thiones, N-Benzyladamantyl-2-imines, and 2-Methyleneadamantanes by Tsai, Tzong-Liang, Chen, Wei-Cheng, Yu, Chin-Hui, le Noble, W. J, Chung, Wen-Sheng

“…The 1,3-dipolar cycloaddition reactions of para-substituted benzonitrile oxides (5-Y) with 5-fluoroadamantane-2-thione (2-F) and -2-methyleneadamantane (3-F)…”
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Geometric equivalents of enantiomers in studies of the stereochemical course of substitution at carbon. Electronic effects in nucleophilic addition to carbonyl groups and to carbocations. Virtual proof of the existence of .sigma. participation by unstrained carbon-carbon bonds by Cheung, C. K, Tseng, L. T, Lin, M. H, Srivastava, S, Le Noble, W. J

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Face Selection in Addition and Elimination in Sterically Unbiased Systems by Kaselj, Mira, Chung, Wen-Sheng, le Noble, William J

“…Kaselj et al discuss the most important addition processes and explain the observed configurational preferences by means of transition-state hyperconjugation…”
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The estimation of activation parameters: Corrections and incorrections by Hamann, S. D, le Noble, W. J

“…Since liquids undergo thermal expansion and hydrostatice compression, expressing concentrations in terms of molarity can cause problems…”
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Effect of pressure on two cyclodextrin-promoted ester hydrolyses by Le Noble, W. J, Srivastava, S, Breslow, R, Trainor, G

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Hyperconjugation as a factor in face selectivity during cycloaddition by Chung, Wen Sheng, Turro, N. J., Srivastava, Sushil, Li, Haifang, Le Noble, W. J.

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Pressure effect on the product distribution in competing reactions: formation of a bis Diels-Alder adduct via an aromatizable intermediate by Srivastava, S, Marchand, A. P, Vidyasagar, V, Flippen-Anderson, J. L, Gilardi, R, George, C, Zachwieja, Z, Le Noble, W. J

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Effect of pressure on the rates of sigmatropic shifts. Volume as an indication of a wide mechanistic range by Schulman, E. M, Merbach, A. E, Turin, M, Wedinger, R, Le Noble, W. J

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Effects of Substituent Modification on Face Selection in Reduction by Jones, Cheryl D, Kaselj, Mira, Salvatore, Ralph N, le Noble, William J

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Face Selectivity in the 1,3-Dipolar Cycloaddition Reactions of Benzonitrile Oxide with 5-Substituted Adamantane-2-thiones and 2-Methyleneadamantanes by Chung, Wen-Sheng, Tsai, Tzong-Liang, Ho, Chia-Chin, Chiang, M. Y. N, le Noble, W. J

“…The 1,3-dipolar cycloaddition reactions of benzonitrile oxide with 5-substituted adamantane-2-thiones (2-X) and 2-methyleneadamantanes (3-X) produced two…”
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Kinetics of reactions in solutions under pressure. 52. Effect of pressure on concerted and stepwise sigmatropic shifts by Le Noble, W. J, Daka, M. Rajaona

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Kinetics of reactions in solutions under pressure. XXX. Special effect of pressure on highly hindered reactions as a possible manifestation of the Hammond postulate by Le Noble, W. J, Asano, T

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The Effect of Pressure on the Rates of Acid-Catalyzed Hydrolysis of Trimethylene Oxide and of Epichlorohydrin by Noble, W. J. le, Duffy, M

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Stereochemistry of reduction and methylation of 5-(trimethylsilyl)adamantan-2-one and 5-(trimethylstannyl)adamantan-2-one by Xie, Mei, Le Noble, W. J

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Reactions in compressed solutions. 56. Evidence for a carbene-anion pair. 1,4-Disubstituted adamantanes as a stereochemical probe by Le Noble, W. J, Chiou, Der-Ming, Okaya, Y

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The Effect of Pressure on the Homogeneous Alkylation of Phenoxide Ion by Le Noble, W. J

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