hippolachnin-a has been researched along with quadricyclane* in 1 studies
1 other study(ies) available for hippolachnin-a and quadricyclane
Article | Year |
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Collaborative Total Synthesis: Routes to (±)-Hippolachnin A Enabled by Quadricyclane Cycloaddition and Late-Stage C-H Oxidation.
Described herein are synthetic efforts toward the synthesis of hippolachnin A. Two independently devised routes from the Brown and Wood groups allowed for the synthesis of hippolachnin A from the unusual starting material, quadricyclane, by harnessing the power of late-stage C-H oxidation. Collaborative union of the best features of the two routes allowed for preparation of the molecule with improved efficiency. Topics: Bridged-Ring Compounds; Carbon; Cycloaddition Reaction; Hydrogen; Molecular Conformation; Oxidation-Reduction; Polyketides; Stereoisomerism | 2016 |