A very short, efficient and inexpensive synthesis of the prodrug form of SC-54701A - A platelet aggregation inhibitor

被引:22
作者
Cossy, J [1 ]
Schmitt, A [1 ]
Cinquin, C [1 ]
Buisson, D [1 ]
Belotti, D [1 ]
机构
[1] UNIV PARIS 05,CHIM & BIOCHIM PHARMACOL & TOXICOL LAB,CNRS,F-75270 PARIS 06,FRANCE
关键词
D O I
10.1016/S0960-894X(97)00293-X
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A short and efficient synthesis of the prodrug form of SC-54701A has been achieved from (trimethylsilyl)acetylene in 6 steps with an overall yield of 19%. (C) 1997 Elsevier Science Ltd.
引用
收藏
页码:1699 / 1700
页数:2
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