JOURNAL ARTICLE

Chiral Frustrated Lewis Pairs Catalyzed Highly Enantioselective Hydrosilylations of Ketones

Xiao‐Qin LiuQiaotian WangCaifang HanXiangqing FengHaifeng Du

Year: 2019 Journal:   Chinese Journal of Chemistry Vol: 37 (7)Pages: 663-666   Publisher: Wiley

Abstract

Summary of main observation and conclusion A highly enantioselective Piers‐type hydrosilylation of simple ketones was successfully realized using a chiral frustrated Lewis pair of tri‐ tert ‐butylphosphine and chiral diene‐derived borane as catalyst. A wide range of optically active secondary alcohols were furnished in 80%—99% yields with 81%—97% ee's under mild reaction conditions.

Keywords:
Enantioselective synthesis Chemistry Borane Frustrated Lewis pair Hydrosilylation Catalysis Optically active Diene Lewis acids and bases Organic chemistry

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2.18
FWCI (Field Weighted Citation Impact)
50
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0.85
Citation Normalized Percentile
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Citation History

Topics

Organoboron and organosilicon chemistry
Physical Sciences →  Chemistry →  Organic Chemistry
Asymmetric Hydrogenation and Catalysis
Physical Sciences →  Chemistry →  Inorganic Chemistry
Asymmetric Synthesis and Catalysis
Physical Sciences →  Chemistry →  Organic Chemistry

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