Asymmetric Syntheses and Absolute Stereochemistry of 5,6-Dihydro-α-pyrones, A New Class of Potent HIV Protease Inhibitors
- 1 April 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 119 (15) , 3627-3628
- https://doi.org/10.1021/ja963434w
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- HIV‐1 Protease inhibitors: Their development, mechanism of action and clinical potentialReviews in Medical Virology, 1995
- Asymmetric Synthesis of an HIV Protease Inhibitor via a Novel .alpha.-Oxoketene/Ketene [4 + 2] Cycloaddition ReactionJournal of the American Chemical Society, 1994
- Structure-Based Design of HIV Protease Inhibitors: 4-Hydroxycoumarins and 4-Hydroxy-2-pyrones as Non-peptidic InhibitorsJournal of Medicinal Chemistry, 1994
- New procedure for the direct generation of titanium enolates. Diastereoselective bond constructions with representative electrophilesJournal of the American Chemical Society, 1990
- Diastereoselective aldol reactions using .beta.-keto imide derived enolates. A versatile approach to the assemblage of polypropionate systemsJournal of the American Chemical Society, 1990