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
收藏
页码：2941 / 2944
页数：4
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