An elegant approach towards the regioselective synthesis of deazalumazinesthrough nucleophile induced ring transformation reactions of 6-aryl-3-cyano-4-methylthio-2H-pyran-2-ones

Citation
P. Srivastava et al., An elegant approach towards the regioselective synthesis of deazalumazinesthrough nucleophile induced ring transformation reactions of 6-aryl-3-cyano-4-methylthio-2H-pyran-2-ones, SYNTHESIS-S, (4), 2000, pp. 541-544
Citations number
21
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
SYNTHESIS-STUTTGART
ISSN journal
00397881 → ACNP
Issue
4
Year of publication
2000
Pages
541 - 544
Database
ISI
SICI code
0039-7881(200004):4<541:AEATTR>2.0.ZU;2-J
Abstract
Deazalumazines also known as pyrido[2,3-d]pyrimidines (3) have been regiose lectively synthesized through nucleophile induced ring transformation react ions of 6-aryl-3-cyano-4methylthio-2H-pyran-2-ones (1) with 6-amino-1,3-dim ethyluracil (2).