STEREOSELECTIVE MICHAEL ADDITION-REACTIONS OF ACYLATED OXAZOLIDINONES TO ETHYL 3-TRIFLUOROMETHYLACRYLATE

被引:46
作者
YAMAZAKI, T [1 ]
HAGA, J [1 ]
KITAZUME, T [1 ]
机构
[1] TOKYO INST TECHNOL, DEPT BIOENGN, MIDORI KU, YOKOHAMA, KANAGAWA 227, JAPAN
关键词
D O I
10.1246/cl.1991.2175
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Michael addition reactions of acyl oxazolidinones to ethyl 3-trifluoromethylacrylate were found to proceed smoothly with a high degree of diastereo- as well as diastereofacial selectivity at the new carbon-carbon bond.
引用
收藏
页码:2175 / 2178
页数:4
相关论文
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