Chiral Ruthenabicyclic Complexes: Precatalysts for Rapid, Enantioselective, and Wide-Scope Hydrogenation of Ketones-Reference-Cited by-同舟云学术

Chiral Ruthenabicyclic Complexes: Precatalysts for Rapid, Enantioselective, and Wide-Scope Hydrogenation of Ketones

Published:2011-06-23 Issue:28 Volume:133 Page:10696-10699
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Matsumura Kazuhiko¹²,Arai Noriyoshi¹,Hori Kiyoto²,Saito Takao²,Sayo Noboru²,Ohkuma Takeshi¹

Affiliation:

1. Division of Chemical Process Engineering, Faculty of Engineering, Hokkaido University, Sapporo, Hokkaido 060-8628, Japan

2. Corporate Research and Development Division, Takasago International Corporation, 1-4-11 Nishi-Yawata, Hiratsuka, Kanagawa 254-0073, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja202296w

Reference35 articles.

1. Ohkuma, T.; Noyori, R.InThe Handbook of Homogeneous Hydrogenation;de Vries, J. G., Elsevier, C. J., Eds.Wiley-VCH:Weinheim, 2007; Vol.3, pp1105–1163.

2. Arai, N.; Ohkuma, T.InScience of Synthesis: Stereoselective Synthesis 2;Molander, G. A., Ed.Thieme:Stuttgart, 2010; pp9–57.

3. Asymmetric hydrogenation of ketones: Tactics to achieve high reactivity, enantioselectivity, and wide scope

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

5. Asymmetric Hydrogenation of Alkenyl, Cyclopropyl, and Aryl Ketones. RuCl2(xylbinap)(1,2-diamine) as a Precatalyst Exhibiting a Wide Scope

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