DIMETHYLDIOXIRANE EPOXIDATION OF CHALCONE AND ISOFLAVONE GLYCOSIDE ACETATES

被引：0
|
作者：
ADAM, W
JEKO, J
LEVAI, A
NEMES, C
PATONAY, T
机构：
[1] UNIV WURZBURG,INST ORGAN CHEM,D-97074 WURZBURG,GERMANY
[2] ALKALOIDA CHEM CO LTD,H-4440 TISZAVASVARI,HUNGARY
[3] LAJOS KOSSUTH UNIV,DEPT ORGAN CHEM,H-4010 DEBRECEN,HUNGARY
来源：
LIEBIGS ANNALEN | 1995年 / 08期
关键词：
CHALCONES; DIMETHYLDIOXIRANES; EPOXIDES; BETA-GLYCOSIDES; ISOFLAVONES;
D O I：
暂无
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
Epoxides of chalcone and isoflavone glycoside acetates were synthesized in high yields and under mild conditions by using dimethyldioxirane. No enantiofacial selectivity was observed during the epoxidation of the enone system.
引用
收藏
页码：1547 / 1549
页数：3
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