1346164-89-3Relevant academic research and scientific papers
Catalytic oxidation synthesis method of 3-mercaptoindole compounds with disulfide as sulfur source
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Paragraph 0064; 0065; 0067, (2018/09/12)
The invention discloses a catalytic oxidation synthesis method of 3-mercaptoindole compounds with disulfide as a sulfur source. The method comprise steps as follows: indole compounds and disulfide aretaken as reaction substrates, potassium iodide and sodi
Metal-free, iodine-catalyzed regioselective sulfenylation of indoles with thiols
Yi, Shanli,Li, Meichao,Mo, Weimin,Hu, Xinquan,Hu, Baoxiang,Sun, Nan,Jin, Liqun,Shen, Zhenlu
, p. 1912 - 1916 (2016/04/19)
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 fea
Iron-facilitated iodine-mediated electrophilic annulation of N,N-dimethyl-2-alkynylanilines with disulfides or diselenides
Du, Hui-Ai,Tang, Ri-Yuan,Deng, Chen-Liang,Liu, Yan,Li, Jin-Heng,Zhang, Xing-Guo
experimental part, p. 2739 - 2748 (2011/12/01)
An efficient synthesis of N-methyl-3-chalcogeno-indoles has been developed via iodine-mediated electrophilic annulation reactions of 2-alkynylaniline derivatives with disulfides or diselenides. In the presence of iodine and iron, a variety of 2-alkynylani
