Enantioselective desymmetrization of cyclopropenes by hydroacylation
- PMID: 21028819
- DOI: 10.1021/ja107738a
Enantioselective desymmetrization of cyclopropenes by hydroacylation
Abstract
We report an enantioselective desymmetrization of cyclopropenes by intermolecular Rh-catalyzed hydroacylation. Cyclopropylketones, bearing quaternary stereocenters, are produced with diastereocontrol (up to >20:1) and excellent enantiomeric excess (up to >99 ee).
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