(R)-(−)- and (S)-(+)-Synadenol: Synthesis, Absolute Configuration, and Enantioselectivity of Antiviral Effect-Reference-Cited by-同舟云学术

(R)-(−)- and (S)-(+)-Synadenol: Synthesis, Absolute Configuration, and Enantioselectivity of Antiviral Effect

Published:1998-12-01 Issue:26 Volume:41 Page:5257-5264
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Qiu Yao-Ling¹,Hempel Andrew¹,Camerman Norman¹,Camerman Arthur¹,Geiser Fiona¹,Ptak Roger G.¹,Breitenbach Julie M.¹,Kira Toshiko¹,Li Ling¹,Gullen Elizabeth¹,Cheng Yung-Chi¹,Drach John C.¹,Zemlicka Jiri¹

Affiliation:

1. Department of Chemistry, Experimental and Clinical Chemotherapy Program, Barbara Ann Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, Michigan 48201-1379, Biochemistry Department, University of Toronto, Toronto, Ontario M5S 1A8, Canada, Ardono Research, Seattle, Washington 98105, Chiral Technologies, Inc., Exton, Pennsylvania 19341, Department of Pharmacology, Yale University School of Medicine, New Haven, Connecticut 06510-8066, and Department of Biologic and Materials...

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm980323u

Reference22 articles.

1. Perchloropolysilane: X-Ray Structure, Solid-State29Si NMR Spectroscopy, and Reactions of [SiCl2]n

2. (R)-(-)- and (S)-(+)-Adenallene: synthesis, absolute configuration, enantioselectivity of antiretroviral effect, and enzymic deamination.

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