Total Synthesis of (−)-Hennoxazole A
- 1 May 1999
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 121 (20) , 4924-4925
- https://doi.org/10.1021/ja9904686
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
- Total Synthesis of (±)-Epilupinine via an Organoyttrium-Catalyzed Sequential Cyclization/Silylation ReactionThe Journal of Organic Chemistry, 1996
- Total Synthesis of the Enantiomer of the Antiviral Marine Natural Product Hennoxazole AJournal of the American Chemical Society, 1995
- (Diethylamino)sulfur Trifluoride (DAST) as a Useful Reagent for the Preparation of 2-Oxazolines from 1,2-Amido AlcoholsHETEROCYCLES, 1995
- Convergent Synthesis of the Polyene Macrolide (-)-RoxaticinJournal of the American Chemical Society, 1994
- Marine natural productsNatural Product Reports, 1993
- Hennoxazoles, bioactive bisoxazoles from a marine spongeJournal of the American Chemical Society, 1991
- A practical and efficient method for enantioselective allylation of aldehydesJournal of the American Chemical Society, 1989
- Application of [2,3] sigmatropic (Wittig) rearrangements in synthesis. The synthesis of (+)-Prelog-Djerassi lactoneJournal of the American Chemical Society, 1985
- ASYMMETRIC REDUCTION OF SIMPLE ACHIRAL KETONES WITH LITHIUM ALUMINUM HYDRIDE PARTIALLY DECOMPOSED BY (−)-N-METHYLEPHEDRINE AND N-ETHYLANILINEChemistry Letters, 1980
- Asymmetric reduction of αβ-unsaturated ketones with lithium aluminium hydride partially decomposed by (–)-N-methylephedrine and N-ethylanilineJournal of the Chemical Society, Chemical Communications, 1980