NOVEL SYNTHESIS OF SUBSTITUTED CIS-BICYCLO[3.3.0]OCTANES VIA PALLADIUM-CATALYZED CYCLIZATION AND SUBSEQUENT BAEYER-VILLIGER RING CLEAVAGE

被引：14

作者：

HEUMANN, A ^{[1
]}

KALDY, S ^{[1
]}

TENAGLIA, A ^{[1
]}

机构：

[1] UNIV AIX MARSEILLE,FAC ST JEROME,CNRS,URA 1411,F-13013 MARSEILLE,FRANCE

来源：

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS | 1993年 / 04期

关键词：

D O I：

10.1039/c39930000420

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The formal transformation of cyclopentadiene to cis-bicyclo[3.3.0]octanes via endo-5-vinyl-2-norbornene involving two different oxidation reactions, such as Pd-catalysed cyclisation and Baeyer-Villiger (BY) ring opening is described.

引用

页码：420 / 422

页数：3

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