| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 5261195 | Tetrahedron Letters | 2016 | 5 Pages | 
Abstract
												An iodine-catalyzed regioselective sulfenylation of indoles in the presence of DMSO has been presented. Various indoles can react with aryl thiols or alkyl thiols to afford their corresponding 3-sulfenylindoles in good to excellent yields. The notable features of this protocol include easy operation, metal-free reaction conditions, and excellent functional group tolerance.178
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											Authors
												Shanli Yi, Meichao Li, Weimin Mo, Xinquan Hu, Baoxiang Hu, Nan Sun, Liqun Jin, Zhenlu Shen, 
											