Tetrahedron letters

Competitive Dienone-Phenol Type Rearrangements for the RegioselectivePreparation of 2, 4-Disubstituted-Naphth-1-ols

JA Dodge, AR Chamberlin

Index: Dodge, Jeffrey A.; Chamberlin, A. Richard Tetrahedron Letters, 1988 , vol. 29, # 38 p. 4827 - 4830

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Citation Number: 12

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. ... The regioselective preparation of 2,4-substituted-naphth-1-ols via a variant of the dienone-phenol rearrangement is described. ... Dienone-phenol type rearrangement of diol 1 under acidic conditions proceeds with fair to excellent regioselectivity to give 2,4-disubstituted-naphth-1-ols (2).