Photooxygenation of 4-(5-methylfuran-2-yl)aminocyanopyridine derivatives


ALTUNDAŞ A., Aslan B. G.

ORGANIC COMMUNICATIONS, vol.11, no.3, pp.163-167, 2018 (ESCI) identifier identifier

  • Publication Type: Article / Article
  • Volume: 11 Issue: 3
  • Publication Date: 2018
  • Doi Number: 10.25135/acg.oc.50.18.09.881
  • Journal Name: ORGANIC COMMUNICATIONS
  • Journal Indexes: Emerging Sources Citation Index (ESCI), Scopus, TR DİZİN (ULAKBİM)
  • Page Numbers: pp.163-167
  • Gazi University Affiliated: Yes

Abstract

One pot syntheses of six-, seven-membered cycloalkane and pyrane junctured aminocyanopyridines bearing furan unit were successfully prepared from the ketones, 2-((5-methylfuran-2-yl)methylene) malononitrile, and ammonium acetate. Photooxygenation of 2-(4-aminocyanopyridine) substituted 5-methylfurans gave 1,4-dicarbonyl functionalized aminocyanopyridine derivatives in good yield in one single operation.