A convenient synthesis of substituted 2-phenylnaphthalenes from phenylacetones

被引：22

作者：

Cotelle, P

Catteau, JP

机构：

[1] Lab. Chim. Organique Phys. A., ENSCL, Université de Lille 1

来源：

TETRAHEDRON LETTERS | 1997年 / 38卷 / 17期

关键词：

D O I：

10.1016/S0040-4039(97)00531-5

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Treatment of phenylacetones 1 with boron tribromide gives the 1,3-dimethyl-2-phenylnaphtalenes 2 in good yields by a tandem aldol condensation-intramolecular Friedel-Crafts cyclization. In the cases of methoxyphenylacetones, a demethylation occurs leading to 1,3-dimethyl-2-hydroxyphenylnaphtols. (C) 1997 Published by Elsevier Science Ltd.

引用

页码：2969 / 2972

页数：4

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