External oxidant-free and selective thiofunctionalization of alkenes enabled by photoredox-neutral catalysis-Reference-Cited by-同舟云学术

External oxidant-free and selective thiofunctionalization of alkenes enabled by photoredox-neutral catalysis

Published:2022 Issue:17 Volume:9 Page:4536-4541
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Liang Rong-Bin¹,Zhu Can-Ming¹,Song Pei-Qi¹,Zhao Lei-Min²^ORCID,Tong Qing-Xiao¹^ORCID,Zhong Jian-Ji¹^ORCID

Affiliation:

1. Department of Chemistry and Key Laboratory for Preparation and Application of Ordered Structural Materials of Guangdong Province, Shantou University, and Chemistry and Chemical Engineering Guangdong Laboratory, Shantou, Guangdong 515063, P. R. China

2. Department of Chemistry, Southern University of Science and Technology (SUSTech), Shenzhen, Guangdong 518055, P. R. China

Abstract

A photoredox approach was reported to realize a highly selective three-component thiohydroxylation, thioalkoxylation and thioamination of vinylarenes towards valuable vicinal S,O- and S,N-disubstituted molecules under mild conditions.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/QO/D2QO00957A

Reference59 articles.

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3. Oxidatively Intercepting Heck Intermediates: Pd-Catalyzed 1,2- and 1,1-Arylhalogenation of Alkenes