Nickel-Catalyzed Reductive Electrophilic Ring Opening of Cycloketone Oxime Esters with Aroyl Chlorides-Reference-Cited by-同舟云学术

Nickel-Catalyzed Reductive Electrophilic Ring Opening of Cycloketone Oxime Esters with Aroyl Chlorides

Published:2018-10-31 Issue:12 Volume:8 Page:11324-11329
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Ding Decai¹,Wang Chuan¹^ORCID

Affiliation:

1. Department of Chemistry, University of Science and Technology of China, Center for Excellence in Molecular Synthesis, Hefei National Laboratory for Physical Science at the Microscale, 96 Jinzhai Road, Hefei, Anhui 20237, P. R. China

Funder

Ministry of Education of the People's Republic of China

National Natural Science Foundation of China

Central People's Government of the People's Republic of China

Publisher

American Chemical Society (ACS)

Subject

Catalysis,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acscatal.8b03930

Reference87 articles.

1. Asymmetric Catalysis of Epoxide Ring-Opening Reactions

2. The Chemistry of Epoxy Alcohols

3. Nucleophilic ring opening of aziridines

4. Asymmetric Ring Opening of Epoxides

5. Synthesis of 1,2-Difunctionalized Fine Chemicals through Catalytic, Enantioselective Ring-Opening Reactions of Epoxides

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