Utilization of wieland furoxan synthesis for preparation of 4-aryl-1,2,5-oxadiazole-3-yl carbamate derivatives having potent anti-HIV activity-Reference-Cited by-同舟云学术

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Utilization of wieland furoxan synthesis for preparation of 4-aryl-1,2,5-oxadiazole-3-yl carbamate derivatives having potent anti-HIV activity

Published:1996-08 Issue:16 Volume:6 Page:1993-1996
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Takayama Hiromitsu,Shirakawa Seiichiro,Kitajima Mariko,Aimi Norio,Yamaguchi Kentaro,Hanasaki Yasuaki,Ide Teruhiko,Katsuura Kimio,Fujiwara Masatoshi,Ijichi Katsushi,Konno Kenji,Sigeta Shiro,Yokota Tomoyuki,Baba Masanori

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference10 articles.

1. A novel lead for specific anti-HIV-1 agents: 1-[(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine

2. Inhibition of HIV-1 Replication by a Nonnucleoside Reverse Transcriptase Inhibitor

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