Cyanation and cyanomethylation of trimethylammonium salts <i>via</i> electrochemical cleavage of C–N bonds-Reference-Cited by-同舟云学术

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Cyanation and cyanomethylation of trimethylammonium salts via electrochemical cleavage of C–N bonds

Published:2022 Issue:5 Volume:9 Page:1288-1294
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Kong Xianqiang¹²,Wang Yuchang¹,Chen Yiyi¹,Chen Xiaohui¹,Lin Long²,Cao Zhong-Yan³^ORCID

Affiliation:

1. School of Chemical Engineering and Materials, Changzhou Institute of Technology, Changzhou 213032, China

2. College of Chemistry, Chemical Engineering and Biotechnology, Donghua University, 2999 North Renmin Lu, Shanghai 201620, China

3. College of Chemistry and Chemical Engineering, Henan University, Kaifeng 475004, China

Abstract

A practical and mild electrochemical protocol for cyanation and cyanomethylation of trimethylammonium salts has been developed.

Funder

National Natural Science Foundation of China

Henan University

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/QO/D1QO01858B

Reference61 articles.

1. Nitrile-Containing Pharmaceuticals: Efficacious Roles of the Nitrile Pharmacophore

2. Designer Magnets Containing Cyanides and Nitriles

3. Recent Advances in the Synthesis of Aryl Nitrile Compounds

4. Advances in C–CN Bond Formation via C–H Bond Activation

5. Nitriles as radical acceptors in radical cascade reactions

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