Original Article
TamerK.Khatab, EbrahimAbdel-Ga
Abstract
The 1,4-dipoles generated from two moles of aromatic ketones have been shown to react efficiently with dimethyl cyanamide via a one-pot [4þ+2] annulation at ambient temperature resulting in the diversity oriented synthesis of a novel series of 1,3-oxazine derivatives through MCR protocol in the presence of tetrachlorosilane - zinc chloride as a heterogeneous promoter.