Selectivity in the thiocyanation of 3-al
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Giovanni Palmisano; Elisabetta Brenna; Bruno Danieli; Giordano Lesma; Bruno Vodo
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Article
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1990
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Elsevier Science
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French
⚖ 268 KB
Reaction of anodically generated thiocyanogen (NaSCN, LiClO4, MeCN, Pt, 0.9V vs SCE) with 3-alkylsubstituted indoles results preferentially in iso2hiocyanafion at the indole 2position rather than in the expected thiocyanation.