ORGANOLEAD-MEDIATED ARYLATION OF ALLYL BETA-KETOESTERS - A SELECTIVE SYNTHESIS OF ISOFLAVANONES AND ISOFLAVONES

被引：39

作者：

DONNELLY, DMX ^{[1
]}

FINET, JP ^{[1
]}

RATTIGAN, BA ^{[1
]}

机构：

[1] UNIV PROVENCE,SREP RADICAUX LIBRES & SYNTH LAB,CNRS,CTR ST JEROME,URA 1412,F-13397 MARSEILLE 20,FRANCE

来源：

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 1993年 / 15期

关键词：

D O I：

10.1039/p19930001729

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Arylation of A-ring substituted and unsubstituted 3-allyloxycarbonylchroman-4-ones with aryllead(IV) triacetates followed by selective catalytic deallyloxycarbonylation affords isoflavanones or isoflavones in high overall yields. The highest yield in the arylation step was observed in the reaction of 5,7-dimethoxychroman-4-one with the more hindered 2,4,6-trimethoxyphenyllead triacetate.

引用

页码：1729 / 1735

页数：7

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