SYNTHESIS AND BIOLOGICAL-ACTIVITY OF POLYCYCLIC QUINONES

被引：0

作者：

TOLSTIKOV, GA

SHULTZ, EE

TOLSTIKOVA, TG

机构：

来源：

SIBIRSKII KHIMICHESKII ZHURNAL | 1992年 / 04期

关键词：

D O I：

暂无

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Polycyclic structural analogues of natural quinones (dienonaphtha-, anthra- and naphthacenequinones) have been synthesized by cycloaddition reactions of 2-isopropenyl-2-thiolene-1,1-dioxide with quinones. The cycloadditon reaction of quinones with oxasoles is a route to isoquinolinoquinones or pyrrolonaphthoquinones. Anthra- and- naphthoquinones containing a terpenoid fragment have been synthesized by retro-decomposition of cycloadditon products of levopimaric acid with quinones.

引用

页码：24 / 31

页数：8