Literature DB >> 17464415

An efficient route for the synthesis of a new class of pyrido[2,3-d]pyrimidine derivatives.

Shujiang Tu1, Junyong Zhang, Runhong Jia, Bo Jiang, Yan Zhang, Hong Jiang.   

Abstract

A new reaction of 4-arylidene-3-methylisoxazol-5(4H)-one or 4-arylidene-2-phenyloxazol-5(4H)-one with 2,6-diaminopyrimidin-4(3H)-one is described and a number of new pyrido[2,3-d]pyrimidine-4,7-dione derivatives are synthesized. This protocol has the advantages of good yields, broad substrate scope and simple work-up.

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Year:  2007        PMID: 17464415     DOI: 10.1039/b617201f

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  3 in total

Review 1.  Controlled microwave heating in modern organic synthesis: highlights from the 2004-2008 literature.

Authors:  C Oliver Kappe; Doris Dallinger
Journal:  Mol Divers       Date:  2009-04-21       Impact factor: 2.943

2.  Crystal structure and Hirshfeld surface analysis of (Z)-3-methyl-4-(thio-phen-2-yl-methyl-idene)isoxazol-5(4H)-one.

Authors:  Rima Laroum; Assia Benouatas; Noudjoud Hamdouni; Wissame Zemamouche; Ali Boudjada; Abdelmadjid Debache
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2021-03-12

3.  High diastereoselective amine-catalyzed Knoevenagel-Michael-cyclization-ring-opening cascade between aldehydes, 3-arylisoxazol-5(4H)-ones and 3-aminocyclohex-2-en-1-ones.

Authors:  Anatoly N Vereshchagin; Michail N Elinson; Yuliya E Anisina; Kirill A Karpenko; Alexander S Goloveshkin; Sergey G Zlotin; Mikhail P Egorov
Journal:  Mol Divers       Date:  2018-03-20       Impact factor: 2.943

  3 in total

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