Enzymatic Process for the Synthesis of cis/trans-(1R,5R)-Bicyclo[3.2.0]hept- 6-ylidene-acetate: Solvent Effect and NMR Study-Reference-Cited by-同舟云学术

Enzymatic Process for the Synthesis of cis/trans-(1R,5R)-Bicyclo[3.2.0]hept- 6-ylidene-acetate: Solvent Effect and NMR Study

Published:2006-04-04 Issue:3 Volume:10 Page:655-660
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Yazbeck Daniel¹,Derrick Andrew¹,Panesar Maninder¹,Deese Alan¹,Gujral Anita¹,Tao Junhua¹

Affiliation:

1. Biotransformations Group, Chemical R&D, Pfizer Global R&D, 10578 Science Center Drive, San Diego, California 92121, U.S.A., and Chemical R&D, Pfizer Global R&D, Ramsgate Road, Sandwich, England

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/op0600409

Reference12 articles.

1. (a) Gladwell, I. R.; Pettman, A. J. WO 2004031115.

2. (b) Derrick, A. M. WO 2004031124.

3. Cycloadditions of dichloroketene to olefins and dienes

4. Automated Enzyme Screening Methods for the Preparation of Enantiopure Pharmaceutical Intermediates

5. Comparison of x-ray crystal structures of an acyl-enzyme intermediate of subtilisin Carlsberg formed in anhydrous acetonitrile and in water

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