The photocatalytic selective 1,2-hydroxyacylmethylation of 1,3-dienes with sulfur ylides as the source of alkyl radicals-Reference-Cited by-同舟云学术

The photocatalytic selective 1,2-hydroxyacylmethylation of 1,3-dienes with sulfur ylides as the source of alkyl radicals

Published:2022 Issue:14 Volume:9 Page:3747-3756
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Xu Shuang-Hua¹,Yan Dong-Mei¹,Rao Li¹,Jiang Min²,Wu Ya-Li¹,Xiao Wen-Jing¹^ORCID,Chen Jia-Rong¹³^ORCID

Affiliation:

1. CCNU-uOttawa Joint Research Centre, Key Laboratory of Pesticide & Chemical Biology, Ministry of Education; College of Chemistry, Central China Normal University, 152 Luoyu Road, Wuhan, Hubei 430079, China

2. College of Materials, Chemistry and Chemical Engineering, Hangzhou Normal University, 2318 Yuhangtang Road, Hangzhou 310036, China

3. School of Chemistry and Chemical Engineering, Henan Normal University, 46 East of Construction Road, Xinxiang 453007, China

Abstract

Highly selective 1,2-hydroxyacylmethylation between 1,3-dienes, sulfur ylides, and water involving photoredox catalysis is described.

Funder

Henan Normal University

Project 211

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/D2QO00383J

Reference106 articles.

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2. Catalytic, Asymmetric Sulfur Ylide-Mediated Epoxidation of Carbonyl Compounds: Scope, Selectivity, and Applications in Synthesis

3. Ylide-Initiated Michael Addition−Cyclization Reactions beyond Cyclopropanes

4. Recent advance in sulfur ylide and sulfonium salts chemistry

5. Bond-Forming and -Breaking Reactions at Sulfur(IV): Sulfoxides, Sulfonium Salts, Sulfur Ylides, and Sulfinate Salts

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