Reaction of arylethanals with boron tribromide

被引：14

作者：

Dupont, R ^{[1
]}

Cotelle, P ^{[1
]}

机构：

[1] Univ Lille 1, ENSCL, CNRS, Chim Phys Organ Lab, F-59655 Villeneuve Dascq, France

来源：

TETRAHEDRON LETTERS | 1998年 / 39卷 / 46期

关键词：

boron and compounds; naphthalenes; polycyclic heterocyclic compounds; Friedel-Crafts reactions;

D O I：

10.1016/S0040-4039(98)01895-4

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Treatment of arylethanals 1 with boron tribromide give 2-phenylnaphthalenes 2 or 1,2,9,10-tetrahydro-1,9-epoxydibenzo[a,e]cyclooctenes 3 by a tandem aldol condensation-intramolecular Friedel;Crafts cyclization or a condensation at the O-position followed by a double Friedel-C:rafts alkylation respectively. In all cases, a total demethylation of the methoxy groups occurs. (C) 1998 Elsevier Science Ltd. All rights reserved.

引用

页码：8457 / 8460

页数：4

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