Enantioselective Synthesis of (−)-Terpestacin and (−)-Fusaproliferin: Clarification of Optical Rotational Measurements and Absolute Configurational Assignments Establishes a Homochiral Structural Series-Reference-Cited by-同舟云学术

Enantioselective Synthesis of (−)-Terpestacin and (−)-Fusaproliferin: Clarification of Optical Rotational Measurements and Absolute Configurational Assignments Establishes a Homochiral Structural Series

Published:2002-03-23 Issue:16 Volume:124 Page:4230-4232
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Myers Andrew G.¹,Siu Michael¹,Ren Feng¹

Affiliation:

1. Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja020072l

Reference17 articles.

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3. Stereochemistry and biosynthesis of terpestacin, a new syncytium formation inhibitor

4. Levy, J. A.HIV and the Pathogenesis of AIDS; American Society for Microbiology: Washington, DC, 1998 pp 121−125 and references therein.

5. The First Total Synthesis of (±)-Terpestacin, HIV Syncytium Formation Inhibitor

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