Utilizing hydrolases of opposite enantiopreference for the preparation of both enantiomers of (1R,7aR)-(?)- and (1S,7aS)-(+)-3,6,7,7a-tetrahydro-1-hydroxy-7a-methyl-1H-inden-5(2H)-one-Reference-Cited by-同舟云学术

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Utilizing hydrolases of opposite enantiopreference for the preparation of both enantiomers of (1R,7aR)-(?)- and (1S,7aS)-(+)-3,6,7,7a-tetrahydro-1-hydroxy-7a-methyl-1H-inden-5(2H)-one

Published:2004 Issue:4 Volume:16 Page:267-271
ISSN:0899-0042
Container-title:Chirality
language:en
Short-container-title:Chirality

Author:

Lo Lee-Chiang,Chou Tzyy-Chao,Shie Jung-Jing

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/chir.20023/fullpdf

Reference27 articles.

1. Enzymes in synthetic organic chemistry. Oxford: Elsevier; 1994. p 41-131.

2. Biotransformations in organic chemistry, 4th ed. Berlin: Springer; 2000.

3. A Structural Basis for the Chiral Preferences of Lipases

4. How can the solvent affect enzyme enantioselectivity?

5. A structure-based rationalization of the enantiopreference of subtilisin toward secondary alcohols and isosteric primary amines

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