DIELS-ALDER REACTION OF CYCLOPENTADIENE AND SPIROEPOXY-2,4-CYCLOHEXADIENONES

被引：13

作者：

GESSON, JP

HERVAUD, L

MONDON, M

机构：

[1] Laboratoire de Chimie 12, Associé au CNRS, F-86 022 Poiters, 40, avenue du Recteur Pineau

来源：

TETRAHEDRON LETTERS | 1993年 / 34卷 / 18期

关键词：

D O I：

10.1016/S0040-4039(00)60487-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Diels-Alder reaction of cyclopentadiene with spiroepoxycyclohexadienones obtained by Adler oxidation of salicyl alcohols affords mainly endo-endo adducts. Cope rearrangement of normal-electron-demand adducts and endo-endo inverse-electron-demand addition of 2a with ethylvinyl ether are also shown.

引用

页码：2941 / 2944

页数：4

共 12 条

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