Nickel‐Catalyzed Asymmetric Hydrogenation of 2‐Amidoacrylates-Reference-Cited by-同舟云学术

Nickel‐Catalyzed Asymmetric Hydrogenation of 2‐Amidoacrylates

Published:2020-03-23 Issue:13 Volume:59 Page:5371-5375
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Hu Yawen¹,Chen Jianzhong²^ORCID,Li Bowen²,Zhang Zhenfeng¹,Gridnev Ilya D.³,Zhang Wanbin¹²^ORCID

Affiliation:

1. Shanghai Key Laboratory for Molecular Engineering of Chiral DrugsSchool of PharmacyShanghai Jiao Tong University 800 Dongchuan Road Shanghai 200240 P. R. China

2. School of Chemistry and Chemical EngineeringShanghai Jiao Tong University 800 Dongchuan Road Shanghai 200240 P. R. China

3. Department of ChemistryGraduate School of ScienceTohoku University Aramaki 3-6, Aoba-ku Sendai 980-8578 Japan

Funder

Shanghai Municipal Education Commission

National Natural Science Foundation of China

Science and Technology Commission of Shanghai Municipality

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.201916534

Reference90 articles.

1. Selected examples:

2. Scaleable catalytic asymmetric Strecker syntheses of unnatural α-amino acids

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4. Discovery of a pathway for terminal-alkyne amino acid biosynthesis

5. Highly enantioselective carbene insertion into N–H bonds of aliphatic amines

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