A Practical Synthesis of Nelfinavir, an HIV-Protease Inhibitor, Using a Novel Chiral C4 Building Block: (5R,6S)-2,2-Dimethyl-5-hydroxy-1,3-dioxepan-6-ylammonium Acetate
Author:
Affiliation:
1. Central Pharmaceutical Research Institute, Japan Tobacco, Inc., 1-1, Murasaki-cho Takatsuki Osaka, 569-1125, Japan, and Agouron Pharmaceuticals, Inc., 3565 General Atomics Court, San Diego, California 92121
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo981472n
Reference12 articles.
1. Viracept (Nelfinavir Mesylate, AG1343): A Potent, Orally Bioavailable Inhibitor of HIV-1 Protease
2. Molecular Recognition of Protein−Ligand Complexes: Applications to Drug Design
3. Towards the synthesis of HIV-protease inhibitors. Synthesis optically pure 3-carboxyl-decahydroisoquinolines.
4. A Convenient, Large Scale Synthesis of N-CBZ-(S-Phenyl)-L-Cysteine
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