摘要
简述从四氢吡喃炔丙醇(1)和1-溴-3-氯丙烷(2)开始经七步反应制备7-氰基-3,4-反-环氧庚-1-烯(9)的方法。(9)是合成具有很强抗肿瘤作用的前列腺素J2的中间体。
7Cyano3,4transepoxyhept1en(9) have been synthesized from tetrahydropyranyl propargyl alcohol and 1bromo3chloropropane in seven steps in this paperThe title compound is a key intermediate in the synthesis of prostaglandin J2 possessing antitumor activity
出处
《白求恩医科大学学报》
CSCD
1998年第1期99-101,共3页
Journal of Norman Bethune University of Medical Science