The synthesis of a dipyrido[3,2-b:3′,4′-e][1,4]diazepinone: Convenient access to a C-ring isomer of the HIV-1 reverse transcriptase inhibitor nevirapine-Reference-Cited by-同舟云学术

The synthesis of a dipyrido[3,2-b:3′,4′-e][1,4]diazepinone: Convenient access to a C-ring isomer of the HIV-1 reverse transcriptase inhibitor nevirapine

Published:1995-01 Issue:2 Volume:5 Page:163-166
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Proudfoot John R.

Publisher

Elsevier BV

Subject

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

Reference12 articles.

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

2. Novel non-nucleoside inhibitors of HIV-1 reverse transcriptase. 1. Tricyclic pyridobenzo- and dipyridodiazepinones

3. A novel Smiles rearrangement gives access to the A-ring pyridine isomers of the nevirapine ring system

4. Regioselective ortho lithiation of halopyridines

5. Synthesis ofortho-substituted aminopyridines. Metalation of pivaloylamino derivatives

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