Selectivity in the thiocyanation of 3-alkylindoles: an unexpectedly easy access to 2-isothiocyano derivatives
…, E Brenna, B Danieli, G Lesma, B Vodopivec, G Fiori
Index: Palmisano, Giovanni; Brenna, Elisabetta; Danieli, Bruno; Lesma, Giordano; Vodopivec, Bruno; Fiori, Gorgio Tetrahedron Letters, 1990 , vol. 31, # 49 p. 7229 - 7232
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Citation Number: 10
Abstract
Download full text in PDF Opens in a new window. Article suggestions will be shown in a dialog on return to ScienceDirect. ... Please enable JavaScript to use all the features on this page. ... Reaction of anodically generated thiocyanogen (NaSCN, LiClO 4 , MeCN, Pt, 0.9V vs SCE) with 3-alkylsubstituted indoles results preferentially in isothiocyanation at the indole 2-position rather than in the expected thiocyanation. ... CR Acad. Sci. Ser.C, 272 (1971), p. 609C.A., 75 ...
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