On August 6, 2021, Li, Laiqiang; Hou, Zhong-Wei; Li, Pinhua; Wang, Lei published an article.Recommanded Product: 2-Methoxynaphthalene The title of the article was Site-Selective Electrochemical C-H Cyanation of Indoles. And the article contained the following:
An electrochem. approach for the site-selective C-H cyanation of indoles to form indole-carbonitriles I [R1 = CN, Ph; R2 = Me, CN, C(O)OMe, etc.; R3 = H, 4-Me, 5-F, 6-Cl, etc.; R4 = Me, Bn, i-Pr, etc.] employing readily available TMSCN as cyano source has been developed. The electrosynthesis relied on the tris(4-bromophenyl)amine as a redox catalyst, which achieved better yield and regioselectivity. A variety of C2- and C3-cyanated indoles were obtained in satisfactory yields. The reactions were conducted in a simple undivided cell at room temperature and obviated the need for transition-metal reagent and chem. oxidant. The experimental process involved the reaction of 2-Methoxynaphthalene(cas: 93-04-9).Recommanded Product: 2-Methoxynaphthalene
The Article related to carbonitrile indole green regioselective preparation, indole trimethylsilyl cyanide electrochem cyanation tris bromophenyl amine catalyst, Heterocyclic Compounds (One Hetero Atom): Indoles, Indolizines, Carbazoles, and Other Arenopyrroles and other aspects.Recommanded Product: 2-Methoxynaphthalene
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