brevipolide-h has been researched along with cyclopropane* in 1 studies
1 other study(ies) available for brevipolide-h and cyclopropane
Article | Year |
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Enantioselective synthesis of (+)-brevipolide H.
The enantioselective synthesis of natural brevipolide H is reported for the first time. By way of Sharpless epoxidation of penta-1,4-dien-3-ol, both enantiomerically pure epoxides were converted to the corresponding olefins for cross metathesis. Subsequent transformations, including epoxide ring opening, esterifications, cyclopropanation, oxidation and ring-closing metathesis, provided the target molecule. This synthesis successfully addresses previous shortcomings in preparing brevipolides. Topics: Cyclization; Cyclopropanes; Epoxy Compounds; Esterification; Hyptis; Oxidation-Reduction; Pyrones; Stereoisomerism | 2016 |