Dimerization of sodium enolates of malonic ester and acetylacetone effected by the action of 4-methyl-3, 4-dibromotetrahydropyran

AA Gevorkyan, AS Arakelyan, SV Barsegyan…

Index: Gevorkyan; Arakelyan; Barsegyan; Petrosyan; Panosyan Russian Journal of Organic Chemistry, 2003 , vol. 39, # 8 p. 1204 - 1205

Full Text: HTML

Citation Number: 3

Abstract

It was shown formerly that 4-methyl-3, 4-dibromotetrahydropyran (I) in reactions with a number of nucleophiles formed in succession products of dehydrobromination and substitution, dihydropyrans III [133]. In performing similar reactions with enolates of b- dicarbonyl compounds we revealed an unusual process: formation of [dehydrodimers] V of the initial dicarbonyl compounds. For instance, from malonic ester malonylmalonic ester ( ...