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CuH-catalyzed enantioselective 1,2-reductions of alpha,beta-unsaturated ketones.

ABSTRACT: The first study on a general technology for arriving at valued nonracemic allylic alcohols using asymmetric ligand-accelerated catalysis by copper hydride is described.

SUBMITTER: Moser R

PROVIDER: S-EPMC3365512 | biostudies-literature | 2010 Jun

REPOSITORIES: biostudies-literature

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CuH-catalyzed enantioselective 1,2-reductions of alpha,beta-unsaturated ketones.

Moser Ralph R Bosković Zarko V ZV Crowe Christopher S CS Lipshutz Bruce H BH

Journal of the American Chemical Society 20100601 23

The first study on a general technology for arriving at valued nonracemic allylic alcohols using asymmetric ligand-accelerated catalysis by copper hydride is described. ...[more]

PMID: 20481528

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