A practical synthesis of 5-(chloromethyl)furo[2,3-b]pyridine, a key intermediate for the HIV protease inhibitor, L-754,394-Reference-Cited by-同舟云学术

A practical synthesis of 5-(chloromethyl)furo[2,3-b]pyridine, a key intermediate for the HIV protease inhibitor, L-754,394

Published:1995-07 Issue:4 Volume:32 Page:1283-1287
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:

Author:

Bhupathy M.,Conlon David A.,Wells Kenneth M.,Nelson John R.,Reider Paul J.,Rossen Kai,Sager Jess W.,Volante R. P.,Dorsey Bruce D.,Hoffman Jacob M.,Joseph Sally A.,Mcdaniel Stacey L.

Publisher

Wiley

Subject

Organic Chemistry

Reference14 articles.

1. L-735,524: an orally bioavailable human immunodeficiency virus type 1 protease inhibitor.

2. L-735,524: The Design of a Potent and Orally Bioavailable HIV Protease Inhibitor

3. Highly diastereoselective reaction of a chiral, non-racemic amide enolate with (S)-glycidyl tosylate. Synthesis of the orally active HIV-1 protease inhibitor L-735,524

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