Asymmetric transfer hydrogenation reactions of N-sulfonylimines by using alcohols as hydrogen sources-Reference-Cited by-同舟云学术

Asymmetric transfer hydrogenation reactions of N-sulfonylimines by using alcohols as hydrogen sources

Published:2018 Issue:39 Volume:54 Page:4963-4966
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Yang Fan¹²³⁴,Chen Jingchao¹²³⁴,Shen Guoli¹²³⁴,Zhang Xuexin¹²³⁴,Fan Baomin¹²³⁴⁵^ORCID

Affiliation:

1. YMU-HKBU Joint Laboratory of Traditional Natural Medicine

2. Yunnan Minzu University

3. Kunming

4. China

5. Key Laboratory of Chemistry in Ethnic Medicinal Resources

Abstract

A palladium/zinc co-catalytic system was established and successfully utilized in the asymmetric transfer hydrogenation reactions of N-sulfonylimines with alcohols as hydrogen sources.

Funder

Yunnan Provincial Department of Education

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2018/CC/C8CC01284A

Reference41 articles.

1. Developments in Asymmetric Hydrogenation from an Industrial Perspective

2. Rhodium-catalysed asymmetric hydrogenation as a valuable synthetic tool for the preparation of chiral drugs

3. Homogeneous palladium-catalyzed asymmetric hydrogenation

4. Transition Metal-Catalyzed Enantioselective Hydrogenation of Enamines and Imines

5. Asymmetric Hydrogenation of Nonaromatic Cyclic Substrates

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