Cyclohexenones Through Regioselective Additon of 1 3 Dicarbonyl Compounds to Terpenoid like Bischalcones Synth Commun     
Yazarlar (3)
Esra Findik
Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Prof. Dr. Yakup BUDAK Tokat Gaziosmanpaşa 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 Synthetic Communications
Dergi ISSN 0039-7911 Wos Dergi Scopus Dergi
Dergi Tarandığı Indeksler SCI
Dergi Grubu Q4
Makale Dili İngilizce
Basım Tarihi 01-2009
Cilt No 39
Sayı 20
Sayfalar 3647 / 3656
DOI Numarası 10.1080/00397910902793877
Özet
Terpenoid-like bischalcones (3 and 4) were synthesized from the reaction of α- and β-ionones and benzaldehydes in excellent yields. The Michael addition of 1,3-dicarbonyl compounds to bischalcones (3 and 4) resulted in the formation of cyclohexenones derivatives (10a–d and 14a, b) via regioselective addition of 1,3-dicarbonyls and then cyclization.
Anahtar Kelimeler
Cyclization | cyclohexenones | regioselective addition | terpenoid-like bischalcone