The First Complete Identification of a Diastereomeric Catalyst−Substrate (Alkoxide) Species in an Enantioselective Ketone Hydrogenation. Mechanistic Investigations-Reference-Cited by-同舟云学术

The First Complete Identification of a Diastereomeric Catalyst−Substrate (Alkoxide) Species in an Enantioselective Ketone Hydrogenation. Mechanistic Investigations

Published:2002-03-16 Issue:14 Volume:124 Page:3680-3691
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Daley Christopher J. A.¹,Bergens Steven H.¹

Affiliation:

1. Contribution from the Department of Chemistry, University of Alberta, Edmonton, Alberta T6G 2G2, Canada

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja0102991

Reference18 articles.

1. Asymmetric Hydrogenation of Amino Ketones Using Chiral RuCl2(diphophine)(1,2-diamine) Complexes

2. [Ru((R)-2,2‘-bis(diphenylphosphino)-1,1‘-binaphthyl)(H)(MeCN)(THF)2](BF4), a Catalyst System for Hydrosilylation of Ketones and for Isomerization, Intramolecular Hydrosilylation, and Hydrogenation of Olefins

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