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

ALTUNDAŞ A., Aslan B. G.

ORGANIC COMMUNICATIONS, cilt.11, sa.3, ss.163-167, 2018 (ESCI) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 11 Sayı: 3
  • Basım Tarihi: 2018
  • Doi Numarası: 10.25135/acg.oc.50.18.09.881
  • Dergi Adı: ORGANIC COMMUNICATIONS
  • Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), Scopus, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.163-167
  • Gazi Üniversitesi Adresli: Evet

Özet

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.