DISCRIMINATION BETWEEN ENANTIOTOPIC GROUPS IN A DIELS-ALDER REACTION

被引:19
作者
JONES, PG
WEINMANN, H
WINTERFELDT, E
机构
[1] UNIV HANNOVER,INST ORGAN CHEM,D-30167 HANNOVER,GERMANY
[2] TECH UNIV CAROLO WILHELMINA BRAUNSCHWEIG,INST ANORGAN & ANALYT CHEM,W-3300 BRAUNSCHWEIG,GERMANY
来源
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH | 1995年 / 34卷 / 04期
关键词
ASYMMETRIC SYNTHESES; DIELS-ALDER REACTIONS;
D O I
10.1002/anie.199504481
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The steric demand of an oxygen atom is less than that of a CH2 group in the kinetic resolution of chiral dienophiles with the enantiomerically pure dienes 1 and ent‐1 (R = OCH3). This realization led to the first differentiation between enantiotopic double bonds in a Diels–Alder reaction for the spirolactone 2 and spiroether 3. (Figure Presented.) Copyright © 1995 by VCH Verlagsgesellschaft mbH, Germany
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页码:448 / 450
页数:3
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