Amide-assisted α-C(sp3)–H acyloxyation of organic sulfides to access α-acyloxy sulfides-Reference-Cited by-同舟云学术

Amide-assisted α-C(sp3)–H acyloxyation of organic sulfides to access α-acyloxy sulfides

Published:2021 Issue:18 Volume:8 Page:4974-4979
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Yang Ke¹^ORCID,Dai Shengfei¹,Li Zhi¹,Li Zhengyi¹^ORCID,Sun Xiaoqiang¹

Affiliation:

1. Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, School of Petrochemical Engineering, Changzhou University, Changzhou, Jiangsu 213164, China

Abstract

The direct acyloxyation of 2-(alkylthio)benzamide has been established via an amide-assisted α-C(sp3)–H functionalization in the presence of Selectfluor by using simple carboxylic acid and its corresponding salt as acyloxy sources.

Funder

National Natural Science Foundation of China

Advanced Catalysis and Green Manufacturing Collaborative Innovation Center, Changzhou University

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/QO/D1QO00774B

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