Synthesis and Biological Evaluation of 5-Arylfuro(2,3-d)pyrimidines as Novel Dihydrofolate Reductase Inhibitors.
Author:
Publisher
Pharmaceutical Society of Japan
Subject
Drug Discovery,General Chemistry,General Medicine
Link
http://www.jstage.jst.go.jp/article/cpb1958/47/2/47_2_156/_pdf
Cited by 14 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Efficient synthesis of novel furo[2,3- d ]pyrimidine derivatives under catalyst-free conditions;Tetrahedron Letters;2017-04
2. Efficient one-pot synthesis of novel and diverse furo[2,3- $$d$$ d ]pyrimidinediones and thioxofuro[2,3- $$d$$ d ]pyrimidineones by the rhodium (II) pivalate-catalyzed reactions of cyclic diazo compounds;Molecular Diversity;2013-08-02
3. Expeditious, Metal-Free, Domino, Regioselective Synthesis of Highly Substituted 2-Carbonyl- and 2-Phosphorylfurans by Formal [3+2] Cycloaddition;European Journal of Organic Chemistry;2012-09-25
4. Discovery of novel c-Met kinase inhibitors bearing a thieno[2,3-d]pyrimidine or furo[2,3-d]pyrimidine scaffold;Bioorganic & Medicinal Chemistry;2011-07
5. ChemInform Abstract: Synthesis and Biological Evaluation of 5-Arylfuro[2,3-d]pyrimidines as Novel Dihydrofolate Reductase Inhibitors.;ChemInform;2010-06-13
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