JOURNAL ARTICLE

Enantioselective Hydrosilylation with Chiral Frustrated Lewis Pairs

Dianjun ChenValeri LeichFangfang PanJürgen Klankermayer

Year: 2012 Journal:   Chemistry - A European Journal Vol: 18 (17)Pages: 5184-5187   Publisher: Wiley

Abstract

Frustrated partners: Based on an initial mechanistic investigation, enantioselective hydrosilylation of various imines was accomplished for the first time by using a novel chiral frustrated Lewis pair (FLP) catalyst. High enantioselectivities of up to 87 % were obtained demonstrating the effectiveness of these metal-free chiral catalysts for this transformation (see scheme). Detailed facts of importance to specialist readers are published as "Supporting Information". Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.

Keywords:
Enantioselective synthesis Hydrosilylation Frustrated Lewis pair Catalysis Computer science Chemistry Organic chemistry Lewis acids and bases

Metrics

170
Cited By
10.23
FWCI (Field Weighted Citation Impact)
32
Refs
0.99
Citation Normalized Percentile
Is in top 1%
Is in top 10%

Citation History

Topics

Organoboron and organosilicon chemistry
Physical Sciences →  Chemistry →  Organic Chemistry
Coordination Chemistry and Organometallics
Physical Sciences →  Chemistry →  Organic Chemistry
Boron Compounds in Chemistry
Health Sciences →  Medicine →  Radiology, Nuclear Medicine and Imaging

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