Enantioselective Total Synthesis of the Potent Anti-HIV Agent Neotripterifordin. Reassignment of Stereochemistry at C(16)
- 1 October 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 119 (41), 9929-9930
- https://doi.org/10.1021/ja972549c
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- An Improved One-pot Procedure for the Synthesis of Alkynes from AldehydesSynlett, 1996
- Anti-AIDS agents—XIX. Neotripterifordin, a novel anti-HIV principle from Tripterygium wilfordii: Isolation and structural elucidationBioorganic & Medicinal Chemistry, 1995
- Anti-AIDS Agents, 18. Sodium and Potassium Salts of Caffeic Acid Tetramers from Arnebia euchroma as Anti-HIV AgentsJournal of Natural Products, 1995
- Anti-AIDS Agents, 4. Tripterifordin, a Novel Anti-HIV Principle from Tripterygium wilfordii: Isolation and Structural ElucidationJournal of Natural Products, 1992
- Methanolysis of Dimethyl (1-Diazo-2-oxopropyl) Phosphonate: Generation of Dimethyl (Diazomethyl) Phosphonate and Reaction with Carbonyl CompoundsSynthetic Communications, 1989
- Catalytic asymmetric epoxidation and kinetic resolution: modified procedures including in situ derivatizationJournal of the American Chemical Society, 1987
- Cyclobutene bridgehead olefin route to the American cockroach sex pheromone, periplanone-BJournal of the American Chemical Society, 1984
- Phyllocladan-16β-ol (13β-Kauran-16β-ol)Australian Journal of Chemistry, 1981
- A direct synthesis of Z-trisubstituted allylic alcohols via the Wittig reactionThe Journal of Organic Chemistry, 1980
- A new method for the deoxygenation of secondary alcoholsJournal of the Chemical Society, Perkin Transactions 1, 1975