trans-RuH(η-BH4)(binap)(1,2-diamine): A Catalyst for Asymmetric Hydrogenation of Simple Ketones under Base-Free Conditions-Reference-Cited by-同舟云学术

trans-RuH(η-BH4)(binap)(1,2-diamine): A Catalyst for Asymmetric Hydrogenation of Simple Ketones under Base-Free Conditions

Published:2002-05-15 Issue:23 Volume:124 Page:6508-6509
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Ohkuma Takeshi¹,Koizumi Masatoshi¹,Muñiz Kilian¹,Hilt Gerhard¹,Kabuto Chizuko¹,Noyori Ryoji¹

Affiliation:

1. Nagoya University, Department of Chemistry and Research Center for Materials Science, Chikusa, Nagoya 464-8602, Japan, and Tohoku University, Instrumental Analysis Center for Chemistry, Graduate School of Science, Aoba, Sendai 980-8578, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja026136%2B

Reference13 articles.

1. trans-[RuCl2(phosphane)2(1,2-diamine)] and Chiraltrans-[RuCl2(diphosphane)(1,2-diamine)]: Shelf-Stable Precatalysts for the Rapid, Productive, and Stereoselective Hydrogenation of Ketones

2. Asymmetric Catalysis by Architectural and Functional Molecular Engineering: Practical Chemo- and Stereoselective Hydrogenation of Ketones

3. Preparation of trans-RuH(η1-BH4)L (L = Me6[15]aneS4, Me8[16]aneS4) and oxidation in alcohols to give trans-{Ru(OR)2(anti-Me8[16]aneS4)}+ R = Me, Et). Crystal structures of the hydrido and ethoxo complexes of Me8[16]aneS4

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