Volume 131, Issue 22 p. 7575
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Innenrücktitelbild: Nickel-Catalyzed Asymmetric Hydrogenation of N-Sulfonyl Imines (Angew. Chem. 22/2019)

Bowen Li

Bowen Li

Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai, 200240 P. R. China

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Dr. Jianzhong Chen

Dr. Jianzhong Chen

Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai, 200240 P. R. China

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Dr. Zhenfeng Zhang

Dr. Zhenfeng Zhang

Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai, 200240 P. R. China

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Prof. Ilya D. Gridnev

Prof. Ilya D. Gridnev

Department of Chemistry, Graduate School of Science, Tohoku University, Sendai, 9808578 Japan

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Prof. Wanbin Zhang

Corresponding Author

Prof. Wanbin Zhang

Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai, 200240 P. R. China

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First published: 10 May 2019

Graphical Abstract

Eine Nickel-katalysierte asymmetrische Hydrierung von N-Sulfonyliminen mit H2-Gas als Wasserstoffquelle wurde mit hohen katalytischen Aktivitäten (S/C bis 10 500) und exzellenten Enantioselektivitäten (bis 99.7% ee) realisiert. Nickel-Katalysatoren sind preiswerter als andere Übergangsmetallkatalysatoren (Rh, Ru, Ir, Pd usw.) und hoch attraktiv für die industrielle Produktion von chiralen Aminen. Einzelheiten der Studie erläutern W. Zhang et al. in ihrer Zuschrift auf S. 7407.

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