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
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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.
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页码：24 / 31
页数：8
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