The First Highly Enantioselective Homogeneously Catalyzed Asymmetric Reductive Amination: Synthesis of α-N-Benzylamino Acids-Reference-Cited by-同舟云学术

The First Highly Enantioselective Homogeneously Catalyzed Asymmetric Reductive Amination: Synthesis of α-N-Benzylamino Acids

Published:2003-04-23 Issue:10 Volume:68 Page:4067-4070
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Kadyrov Renat¹,Riermeier Thomas H.¹,Dingerdissen Uwe¹,Tararov Vitali¹,Börner Armin¹

Affiliation:

1. Degussa AG, Project House Catalysis, Industriepark Höchst, G 830, D-65926 Frankfurt/Main, Germany, Leibniz-Institut für Organische Katalyse an der Universität Rostock e.V., Buchbinderstr. 5/6, D-18055 Rostock, Germany, and Fachbereich Chemie der Universität Rostock, A.-Einsteinstr. 3a, D-18059 Rostock, Germany renat.kadyrov@degussa.com; armin.boerner@ifok.uni-rostock.de

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo020690k

Reference24 articles.

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2. (b) Rylander, P. N.Hydrogenation Methods; Academic Press: New York, 1985; pp 82−93.

3. Reductive amination of carbonyl compounds in the presence of cobalt and rhodium complexes

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