Synthesis and evaluation of novel quinolinones as HIV-1 reverse transcriptase inhibitors-Reference-Cited by-同舟云学术

Synthesis and evaluation of novel quinolinones as HIV-1 reverse transcriptase inhibitors

Published:2001-07 Issue:14 Volume:11 Page:1943-1945
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Patel Mona,McHugh Robert J,Cordova Beverly C,Klabe Ronald M,Bacheler Lee T,Erickson-Viitanen Susan,Rodgers James D

Publisher

Elsevier BV

Subject

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

Reference7 articles.

1. Pathogenesis of human immunodeficiency virus infection

2. The HIV-1 Reverse Transcription (RT) Process as Target for RT Inhibitors

3. Nonnucleoside reverse transcriptase inhibitors

4. L-743, 726 (DMP-266): a novel, highly potent nonnucleoside inhibitor of the human immunodeficiency virus type 1 reverse transcriptase

5. For the preparation of MoOPH see: Vedejs, E.; Larsen, S. In Organic Syntheses; Freeman, J. P., Ed.; John Wiley & Sons: New York, 1990; Coll. Vol. 7, pp 277–282.

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