Photooxygenation of 4-(5-methylfuran-2-yl)aminocyanopyridine derivatives
ORGANIC COMMUNICATIONS, cilt.11, sa.3, ss.163-167, 2018 (ESCI, Scopus, TRDizin)
- 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.