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Enantioselective conjugate hydrosilylation of α,β-unsaturated ketones.


ABSTRACT: Enantioselective conjugate hydrosilylation of β,β-disubstituted α,β-unsaturated ketones was realized. In the presence of a chiral picolinamide-sulfonate Lewis base catalyst, the reactions provided various chiral ketones bearing a chiral center at the β-position in up to quantitative yields with moderate enantioselectivities.

SUBMITTER: Yang H 

PROVIDER: S-EPMC9063358 | biostudies-literature | 2019 Apr

REPOSITORIES: biostudies-literature

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Enantioselective conjugate hydrosilylation of α,β-unsaturated ketones.

Yang Huan H   Weng Guanglin G   Fang Dongmei D   Peng Changjiang C   Zhang Yuanyuan Y   Zhang Xiaomei X   Wang Zhouyu Z  

RSC advances 20190412 21


Enantioselective conjugate hydrosilylation of β,β-disubstituted α,β-unsaturated ketones was realized. In the presence of a chiral picolinamide-sulfonate Lewis base catalyst, the reactions provided various chiral ketones bearing a chiral center at the β-position in up to quantitative yields with moderate enantioselectivities. ...[more]

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