Aqueous MCRs of quaternary ammoniums, N-substituted formamides and sodium disulfide towards aryl thioamides-Reference-Cited by-同舟云学术

Aqueous MCRs of quaternary ammoniums, N-substituted formamides and sodium disulfide towards aryl thioamides

Published:2017 Issue:3 Volume:4 Page:413-416
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Zhou Zhou¹²³⁴⁵,Yu Jin-Tao¹²³⁴⁵^ORCID,Zhou Yongnan¹²³⁴⁵,Jiang Yan¹²³⁴⁵,Cheng Jiang¹²³⁴⁵^ORCID

Affiliation:

1. School of Petrochemical Engineering

2. Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology

3. Jiangsu Province Key Laboratory of Fine Petrochemical Engineering

4. Changzhou University

5. Changzhou 213164

Abstract

A three-component reaction of quaternary ammonium salts, N-substituted formamides and aqueous sodium disulfide was developed, leading to aryl/heteroaryl thioamides in moderate to good yields with good functional group compatibility.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/QO/C6QO00670A

Reference53 articles.

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4. N. Kumagai , Reactions using thioamide and allylic cyanide, in Comprehensive Chirality, ed. E. M. Carreira and H. Yamamoto, 2012, vol. 4, p. 293

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