Visible-Light-Initiated Catalyst-Free Radical Annulation Reactions of 1,6-Enynes and Aryl Sulfonyl Bromide to Assemble Sulfonation/Bromination Succinimide Derivatives
Author:
Affiliation:
1. Jiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials, School of Chemistry and Materials Science, Jiangsu Normal University, Xuzhou, Jiangsu 221116, P. R. China
Funder
Natural Science Research of Jiangsu Higher Education Institutions of China
National Natural Science Foundation of China
Publisher
American Chemical Society (ACS)
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c02693
Reference42 articles.
1. K2S2O8-Mediated Radical Cyclization of 1,6-Enyne for the Synthesis of Diiodonated γ-Lactams
2. Time-Economical Radical Cascade Cyclization/Haloazidation of 1,6-Enynes: Construction of Highly Functional Succinimide Derivatives
3. Photocatalytic Decarboxylative [2 + 2 + m] Cyclization of 1,7-Enynes Mediated by Tricyclohexylphosphine and Potassium Iodide
4. Catalytic Dual 1,1-H-Abstraction/Insertion for Domino Spirocyclizations
5. Energy Economical Annulation Reaction of 1,6‐Enynes with Thiosulfonates (Selenosulfonates): Efficient Synthesis of Multisubstituted Pyrrolidine Derivatives under Room Temperature
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1. Recent progress in visible light‐driven halogenation: Chlorination, bromination, and iodination;Bulletin of the Korean Chemical Society;2024-09-03
2. Copper‐Catalyzed Radical‐Induced Annulation‐Halo(bi)cyanomethylation of Indole‐Tethered 1,6‐Enynes toward Pyrrolo[1,2‐a]indoles;Advanced Synthesis & Catalysis;2024-08-05
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