Visible-light-induced sulfonylarylation of unactivated alkenes via 1,4-(hetero)aryl migration from oxygen or nitrogen to carbon
Author:
Affiliation:
1. State Key Laboratory of Elemento-Organic Chemistry, Research Institute of Elemento-Organic Chemistry, College of Chemistry, Frontiers Science Center for New Organic Matter, Nankai University, Tianjin 300071, China
Abstract
Funder
Nankai University
National Natural Science Foundation of China
Publisher
Royal Society of Chemistry (RSC)
Subject
Pollution,Environmental Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2022/GC/D2GC03187F
Reference54 articles.
1. Olefinic C–H functionalization through radical alkenylation
2. An Electrocatalytic Approach to the Radical Difunctionalization of Alkenes
3. Strategies toward Dicarbofunctionalization of Unactivated Olefins by Combined Heck Carbometalation and Cross-Coupling
4. Recent advances in copper-catalysed radical-involved asymmetric 1,2-difunctionalization of alkenes
5. Visible-light-mediated three-component Minisci reaction for heteroarylethyl alcohols synthesis
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