SYNTHESIS OF THE DOPAMINE AGONIST (-)-QUINPIROLE

被引：20

作者：

SCHAUS, JM

HUSER, DL

TITUS, RD

机构：

[1] Lilly Research Laboratories, Indianapolis, IN, 46285, Eli Lilly and Company

来源：

SYNTHETIC COMMUNICATIONS | 1990年 / 20卷 / 22期

关键词：

D O I：

10.1080/00397919008051599

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A convenient synthesis and resolution of (-)-trans-4aR,8aR-1-propyl-6-oxo-decahydroquinoline (4) is described. This compound is then converted into the D-2 selective dopamine agonist, (-)-quinpirole hydrochloride (3).

引用

页码：3553 / 3562

页数：10

共 8 条

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