Two-parameter Analysis of Solvent Effects on Selectivity in Chemical Reactions: Information of Polarity and Activation Volume at the Transition State in Organic and Enzymatic Reactions
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
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1. Complementary Lewis acid-base description of solvent effects. I. Ion-ion and ion-dipole interactions
2. Is the tert-Butyl Chloride Solvolysis the Most Misunderstood Reaction in Organic Chemistry? Evidence Against Nucleophilic Solvent Participation in the tert-Butyl Chloride Transition State and for Increased Hydrogen Bond Donation to the 1-Adamantyl Chloride Solvolysis Transition State
3. A new approach to preparative enzymatic synthesis
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5. Rules for optimization of biocatalysis in organic solvents
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