Facile and efficient synthesis of acridinediones from primary amino alcohols via three-component condensation reactions assisted by microwave irradiation

Abdelhamid, Antar; Mohamed, S.K.; Maharramov, A.M.; Xəlilov, Əli; Allahverdiev, M.A.

doi:10.1016/j.jscs.2011.10.005

Facile and efficient synthesis of acridinediones from primary amino alcohols via three-component condensation reactions assisted by microwave irradiation

istinad üçün kopyala

Abdelhamid A. A., Mohamed S., Maharramov A., Xəlilov Ə., Allahverdiev M.

Journal of Saudi Chemical Society, vol.18, no.5, pp.474-478, 2014 (SCI-Expanded)

Nəşrin Növü: Article / Article
Cild: 18 Say: 5
Nəşr tarixi: 2014
Doi nömrəsi: 10.1016/j.jscs.2011.10.005
jurnalın adı: Journal of Saudi Chemical Society
Jurnalın baxıldığı indekslər: Science Citation Index Expanded (SCI-EXPANDED), Scopus
Səhifə sayı: pp.474-478
Açar sözlər: Acridinediones, Amino alcohols, Microwave irradiation, One pot, Three component reactions, β-Diketone
Adres: Bəli

Qısa məlumat

Microwave irradiation of three component reaction of dimedone, appropriate aromatic aldehydes and amino alcohols in a stoichiometrical ratio 2:1:1 for few minutes afforded the formation of a stable fused three membered ring of the corresponding 3,6,6-tetramethyl-2,3,4,5,6,7,8,9,10-decahydroacridine-1,8-dione derivatives in an excellent yield (80-91%). The structure of all products has been characterized by X-ray crystal structural analyses, 13C NMR, 1H NMR, IR and mass spectrum analyses.