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Synthesis of highly enantio-enriched stereoisomers of hydroxy-GR24†
J. C. Morris,C. S. P. McErlean
Organic & Biomolecular Chemistry Pub Date : 12/15/2015 00:00:00 , DOI:10.1039/C5OB02349A
Abstract

In contrast to a biomimetic electrophilic cyclisation cascade, we employ a contra-biomimetic nucleophilic cyclisation cascade to give the tricyclic core of 4-hydroxy-GR24 in a single step. Kinetic resolution using a stereoselective Noyori transfer hydrogenation enables the concise synthesis of any enantiomerically enriched 4-hydroxy-GR24 stereoisomer.

Graphical abstract: Synthesis of highly enantio-enriched stereoisomers of hydroxy-GR24
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