<i>N</i>-Sulfenyl phthalimide enabled Markovnikov hydrothiolation of unactivated alkenes <i>via</i> ligand promoted cobalt catalysis-Reference-Cited by-同舟云学术

N-Sulfenyl phthalimide enabled Markovnikov hydrothiolation of unactivated alkenes via ligand promoted cobalt catalysis

Published:2024 Issue:3 Volume:11 Page:646-653
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Li Xiang-Rui¹^ORCID,Zhang Rong-Jin¹,Xiao Yonghong¹^ORCID,Tong Qing-Xiao¹^ORCID,Zhong Jian-Ji¹²^ORCID

Affiliation:

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

2. Chemistry and Chemical Engineering Guangdong Laboratory, Shantou 515063, P. R. China

Abstract

N-Sulfenyl phthalimides as efficient radicalophile reagents is herein reported to enable the Markovnikov hydrothiolation of unactivated alkenes by cobalt catalysis with exclusive regio-selectivity and wide functional group tolerance.

Funder

Basic and Applied Basic Research Foundation of Guangdong Province

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D3QO01632C

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