Helvetica Chimica Acta

Controlled allylic transformations via the Meisenheimer rearrangement

V Rautenstrauch

Index: Rautenstrauch,V. Helvetica Chimica Acta, 1973 , vol. 56, p. 2492 - 2508

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Citation Number: 29

Abstract

Abstract Described are synthetic sequences which effect allylic transformations I and II. Sequence I involves (1) conversion of a primary allyl alcohol into the corresponding N, N- dimethyl-amine oxide,(2)[2, 3]-rearrangement to give an N, N-dimethylhydroxylamine and (3a) reduction to give the 'rearranged'secondary or tertiary allyl alcohol [eg 36 [RIGHTWARDS ARROW] 35 [RIGHTWARDS ARROW] 37 [RIGHTWARDS ARROW] 40]. ...