Three Step Synthesis of 2 4 Diaryl 5 6 7 8 tetrahydroquinolineDerivatives    
Yazarlar (3)
Hayreddin Gezegen
Cumhuriyet Üniversitesi, Türkiye
Alparslan Atahan
Düzce Üniversitesi, Türkiye
Prof. Dr. Mustafa CEYLAN Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Makale Türü Özgün Makale
Makale Alt Türü SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale
Dergi Adı JOURNAL OF HETEROCYCLIC CHEMISTRY
Dergi ISSN 0022-152X Wos Dergi Scopus Dergi
Dergi Tarandığı Indeksler SCI-Expanded
Dergi Grubu Q4
Makale Dili İngilizce
Basım Tarihi 09-2010
Cilt No 47
Sayı 5
Sayfalar 1017 / 1024
DOI Numarası 10.1002/jhet.409
Özet
Addition of cylohexanone to chalcones, obtained from the appropriate acetophenone and benzaldehyde derivatives, under solvent‐free conditions gave 1,5‐diketones in good yields. Treatment of 1,5‐diketones with ammonium acetate in acetic acid afforded directly 2,4‐diaryl‐5,6,7,8‐tetrahydroquinoline derivatives 7a, 7b, 7c, 7d, 7e, 7f, 7g, 7h, 7i, 7j, 7k, 7l, 7m, 7n, 7o, 7p, 7r, 7s, 7t, 7u in high yields. The structures of 7a, 7b, 7c, 7d, 7e, 7f, 7g, 7h, 7i, 7j, 7k, 7l, 7m, 7n, 7o, 7p, 7r, 7s, 7t, 7u were elucidated by 1H NMR, 13C NMR, IR, and elemental analysis. J. Heterocyclic Chem., (2010).
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