Tricyclic Quinazoline Alkaloids: Isolation, Synthesis, Chemical Modification, and Biological Activity

被引：51
作者：
Shakhidoyatov, Kh M. [1 ]
Elmuradov, B. Zh [1 ]
机构：
[1] Acad Sci Uzbek, S Yu Yunusov Inst Chem Plant Subst, Tashkent, Uzbekistan
来源：
CHEMISTRY OF NATURAL COMPOUNDS | 2014年 / 50卷 / 05期
关键词：
quinazoline alkaloids; deoxyvasicinone; deoxypeganine; peganol; mackinazoline; mackinazolinone; luotonin A; B; and E; rutaecarpine; isaindigotone; synthesis; transformation; activity; REDUCTIVE N-HETEROCYCLIZATION; NITROGEN BRIDGEHEAD COMPOUNDS; SOLID-PHASE SYNTHESIS; ONE-POT SYNTHESIS; LUOTONIN-A; ADHATODA-VASICA; EFFICIENT SYNTHESIS; ALPHA-AMINATION; ISAINDIGOTONE DERIVATIVES; OXIDATIVE REARRANGEMENT;
D O I：
10.1007/s10600-014-1086-6
中图分类号：
R914 [药物化学];
学科分类号：
100701 ;
摘要：
Results of the last 15-20 years on the isolation, synthesis, chemical modification, and biological activity of natural tricyclic quinazolines and their synthetic analogs were reviewed.
引用
收藏
页码：781 / 800
页数：20
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