INTRAMOLECULAR DIELS-ALDER REACTION OF 1-ETHOXYCARBONYL-4-ALKENYLCYCLOPENTADIENES

被引：8

作者：

HIMEDA, Y

HIRATANI, K

HATANAKA, M

UEDA, I

机构：

[1] OSAKA UNIV,INST SCI & IND RES,IBARAKI,OSAKA 567,JAPAN

[2] IND PROD RES INST,TSUKUBA,IBARAKI 305,JAPAN

来源：

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS | 1992年 / 22期

关键词：

D O I：

10.1039/c39920001684

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

4-(But-3-enyl)- and 4-(pent-4-enyl)-l-ethoxycarbonyl-2-ethoxycyclopentadiene, prepared from allylidenetriphenylphosphorane and alpha-haloketones, underwent a regioselective intramolecular Diels-Alder reaction to give two types of the functionalized tricyclic products depending on the linking carbon-chain length.

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页码：1684 / 1685

页数：2

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