Enzyme-Catalyzed Hydrolysis of Bicycloheptane and Cyclobutene Diesters to Monoesters-Reference-Cited by-同舟云学术

Enzyme-Catalyzed Hydrolysis of Bicycloheptane and Cyclobutene Diesters to Monoesters

Published:2013-11-15 Issue:6 Volume:18 Page:774-780
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Guo Zhiwei¹,Wong Michael Kwok Y.¹,Hickey Matthew R.¹,Patel Bharat P.¹,Qian Xinhua¹,Goswami Animesh¹

Affiliation:

1. Chemical Development, Bristol-Myers Squibb, New Brunswick, New Jersey 08903, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/op400254c

Reference23 articles.

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2. Mechanistic definition of trimethylstannylation of 1,4-dihalobicyclo[2.2.1]heptanes: bridgehead nucleophilic substitution mediated by the intermediacy of radicals, radical anions, carbanions, and [2.2.1.]propellane

3. Decarboxylation of Bridgehead Carboxylic Acids by the Barton Procedure

4. Qian, X.; Ramirez, A.; Wong, M. K. Y.; Yamamoto, K.; Fox, R.; Guo, Z.; Goswami, A.; Patel, B.; Cann, R. O.; Deshpande, R. P.Presented at the 240th ACS National Meeting, Boston, MA, Aug 22–26, 2010.

5. Design, Synthesis, Radiolabeling, and in Vitro and in Vivo Evaluation of Bridgehead Iodinated Analogues of N-{2-[4-(2-Methoxyphenyl)piperazin-1-yl]ethyl}-N-(pyridin-2-yl)cyclohexanecarboxamide (WAY-100635) as Potential SPECT Ligands for the 5-HT1A Receptor

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