Design and synthesis of angucyclinone AB-pyrido[2,3-d] pyrimidine analogues
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Date
2008
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PERGAMON-ELSEVIER SCIENCE LTD
Abstract
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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Keywords
quinones, Michael addition, diels-alder reaction, regioselectivity, IN-VITRO, CYTOTOXICITY, APOPTOSIS, PHOTOCHEMISTRY, ANTIBIOTICS