Design and synthesis of angucyclinone AB-pyrido[2,3-d] pyrimidine analogues

被引:16
|
作者
Valderrama, Jaime A. [1 ]
Vasquez, David [1 ]
机构
[1] Pontificia Univ Catolica Chile, Fac Quim, Santiago, Chile
关键词
quinones; Michael addition; diels-alder reaction; regioselectivity;
D O I
10.1016/j.tetlet.2007.11.133
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The preparation of two pyrimido[4,5-c]isoquinoline-7, 10-quinones from acylhydroquinones and 1,3-dimethyl-5-aminouracil and their cycloadditions with 1-trimethylsilyloxybutadiene and 1-dimethylamino-3-methyl-1-azabutadiene is described. The remarkable regio-control of these cycloadditions that yield stable 1:1 cycloadducts is discussed on the basis of steric interactions into the pyrimido[4,5-c]isoquinoline-7,10-quinones. The access to angucyclinone AB-pyridopyrimidine analogues from Diels-Alder adducts and preliminar evidences on their antitumour activities are also reported. (c) 2007 Elsevier Ltd. All rights reserved.
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页码:703 / 706
页数:4
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