Effects of Chiral Additives on Enantioselectivity for Lipase-Catalyzed Esterifications in an Organic Solvent. A Remarkable Enhancement of Its Enantioselectivity Due to Cooperative Effects of Two Kinds of Additives-Reference-Cited by-同舟云学术

Effects of Chiral Additives on Enantioselectivity for Lipase-Catalyzed Esterifications in an Organic Solvent. A Remarkable Enhancement of Its Enantioselectivity Due to Cooperative Effects of Two Kinds of Additives

Published:2002-10 Issue:10 Volume:75 Page:2239-2240
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Ueji Shin-ichi,Sakamoto Hideyuki,Watanabe Keiichi,Okamoto Takashi,Mori Shuichi

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference12 articles.

1. Salts dramatically enhance activity of enzymes suspended in organic solvents

2. Crown Ethers as Regulators of Enzymatic Reactions: Enhanced Reaction Rate and Enantioselectivity in Lipase-Catalyzed Hydrolysis of 2-Cyano-1-methylethyl Acetate

3. Thiacrown Ether Technology in Lipase-Catalyzed Reaction: Scope and Limitation for Preparing Optically Active 3-Hydroxyalkanenitriles and Application to Insect Pheromone Synthesis

4. Enantioselectivity Related to Conformational Changes Observed by Spectral Analysis in Subtilisin-Catalyzed Hydrolysis of Ethyl (RS)-2-(4-Substituted Phenoxy)Propionates

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