Chemoenzymatic synthesis of (–)-carbovir utilizing a whole cell catalysed resolution of 2-azabicyclo[2.2.1]hept-5-en-3-one-Reference-Cited by-同舟云学术

Chemoenzymatic synthesis of (–)-carbovir utilizing a whole cell catalysed resolution of 2-azabicyclo[2.2.1]hept-5-en-3-one

Published:1990 Issue:16 Volume: Page:1120-1121
ISSN:0022-4936
Container-title:J. Chem. Soc., Chem. Commun.
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Taylor Steven J. C.,Sutherland Alan G.,Lee Carol,Wisdom Richard,Thomas Steve,Roberts Stanley M.,Evans Christopher

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1990/C3/C39900001120

Reference10 articles.

1. Carbocyclic nucleosides

2. Synthesis and enzymatic resolution of carbocyclic 2′-ara-fluoro-guanosine: a potent new anti-herpetic agent

3. Comparison of the effect of Carbovir, AZT, and dideoxynucleoside triphosphates on the activity of human immunodeficiency virus reverse transcriptase and selected human polymerases

4. C. Williamson , A. M.Exall, M. F.Jones, C. L.Mo, P. L.Myers, I. L.Paternoster, and R.Storey, Poster presentation at SCI Medicinal Chemistry Symposium, Cambridge, 1989.

5. Synthesis and antiviral activity of the enantiomeric forms of carba-5-iodo-2'-deoxyuridine and carba-(E)-5-(2-bromovinyl)-2'-deoxyuridine

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