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Open Chemistry

formerly Central European Journal of Chemistry

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IMPACT FACTOR 2016 (Open Chemistry): 1.027
IMPACT FACTOR 2016 (Central European Journal of Chemistry): 1.460

CiteScore 2017: 1.45

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2391-5420
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Volume 9, Issue 1

Issues

Volume 13 (2015)

Asymmetric transfer hydrogenation of prochiral ketones catalyzed by aminosulfonamide-ruthenium complexes in ionic liquid

Zhongqiang Zhou
  • Key Laboratory of Catalysis and Materials Science of the State Ethnic Affairs Commission & Ministry of Education, College of Chemistry and Materials Science, South-Central University for Nationalities, Wuhan, 430074, China
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/ Yong Sun
  • Key Laboratory of Catalysis and Materials Science of the State Ethnic Affairs Commission & Ministry of Education, College of Chemistry and Materials Science, South-Central University for Nationalities, Wuhan, 430074, China
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  • Other articles by this author:
  • De Gruyter OnlineGoogle Scholar
/ Aiqing Zhang
  • Key Laboratory of Catalysis and Materials Science of the State Ethnic Affairs Commission & Ministry of Education, College of Chemistry and Materials Science, South-Central University for Nationalities, Wuhan, 430074, China
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Published Online: 2010-12-16 | DOI: https://doi.org/10.2478/s11532-010-0134-8

Abstract

Chiral aminosulfonamides containing imidazolium group were used as ligands for the ruthenium(II)-catalyzed asymmetric transfer hydrogenation of prochiral ketones in ionic liquid, affording good to excellent conversions and enantiomeric excesses. The catalytic system could be easily recovered and reused several times.

Keywords: Asymmetric transfer hydrogenation; Aminosulfonamide; Ionic liquid; Ketones

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About the article

Published Online: 2010-12-16

Published in Print: 2011-02-01


Citation Information: Open Chemistry, Volume 9, Issue 1, Pages 175–179, ISSN (Online) 2391-5420, DOI: https://doi.org/10.2478/s11532-010-0134-8.

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© 2011 Versita Warsaw. This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License. BY-NC-ND 3.0

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