Manipulation of enzymic regioselectivity by structural modification of substrates
SH Wu, LC Lo, ST Chen, KT Wang
Index: Wu, Shih-Hsiung; Lo, Lee-Chiang; Chen, Shui-Tein; Wang, Kung-Tsung Journal of Organic Chemistry, 1989 , vol. 54, # 17 p. 4220 - 4222
Full Text: HTML
Citation Number: 16
Abstract
L-Asp diester L-Ais-2 nonoester cation has attracted attention of the organic chemists because of their usefulness as chiral catalysk2 For organic reactions, selectivity such as enantioselectivity, diastereoselectivity, and regioselectivity is one of the challenges3 and may often be overcome by biocatalytic reaction^.^ In this article, we describe novel observations which demonstrate that either the a-or@-ester of L-aspartic acid diester may ...
Related Articles:
Stabilized analogs of thymopentin. 2. 1, 2-and 3, 4-ketomethylene pseudopeptides
[Journal of Medicinal Chemistry, , vol. 40, # 15 p. 2398 - 2406]
Manipulation of enzymic regioselectivity by structural modification of substrates
[Journal of Organic Chemistry, , vol. 54, # 17 p. 4220 - 4222]