ASYMMETRIC DIELS-ALDER REACTION OF A CHIRAL AZLACTONE

被引：17

作者：

BUNUEL, E ^{[1
]}

CATIVIELA, C ^{[1
]}

DIAZDEVILLEGAS, MD ^{[1
]}

机构：

[1] UNIV ZARAGOZA,CSIC,INST CIENCIA MAT ARAGON,DEPT QUIM ORGAN,E-50009 ZARAGOZA,SPAIN

来源：

TETRAHEDRON-ASYMMETRY | 1994年 / 5卷 / 02期

关键词：

D O I：

10.1016/S0957-4166(00)86161-3

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The chilal Z-azlactone derived from 1,2-O-isopropylidene-D-glyceraldehyde underwent facial diastereoselective Diels-Alder reaction with cyclopentadiene. Catalyst and temperature dependence of the product ratio is described The absolute configuration of the major compound was established by an X-ray crystallographic analysis.

引用

页码：157 / 160

页数：4

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