STEREOSELECTIVE SYNTHESIS OF A NEW ALDOSE REDUCTASE INHIBITOR - AN EXTENSION OF THE BISLACTIM ETHER METHOD FOR THE SYNTHESIS OF AMINO-ACIDS

被引:4
作者
GLOMBIK, H
机构
[1] Hoechst AG
关键词
D O I
10.1016/S0040-4020(01)90071-7
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The stereoselective synthesis of the imidazolidinedione (+)-2, an inhibitor of aldose reductase, has been achieved via heterocyclic bislactim ether substitution, acidic cleavage and cyclization with urea. © 1990.
引用
收藏
页码:7745 / 7750
页数:6
相关论文
共 13 条