Synlett

Indium (III) chloride-catalyzed coupling reaction of acid chlorides and allylic tins

K Inoue, Y Shimizu, I Shibata, A Baba

Index: Inoue; Shimizu; Shibata; Baba Synlett, 2001 , # 10 p. 1659 - 1661

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Citation Number: 9

Abstract

Abstract: Allylic tributyltins and acid chlorides are effectively coupled to yield allylic ketones in indium (III) chloride-catalyzed reactions. In the case of g-unsubstituted allylic tins, the assistance of a phosphine is essential to prevent further allylation of the produced ketones. Key words: indium, allylic tin, acid chloride, phosphine, coupling reaction

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~71%

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