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作 者:Hela Slimi Khemais Said Younes Moussaoui Ridha Ben Salem
机构地区:[1]Physical Organic Chemistry Laboratory(UR11ES74),Science Faculty of Sfax,Sfax University,Sfax,Tunisia [2]Science Faculty of Gafsa,Gafsa University,Gafsa,Tunisia
出 处:《International Journal of Organic Chemistry》2013年第3期96-100,共5页有机化学国际期刊(英文)
基 金:financial support of the Ministry of Higher Education and Scientific Research of Tunisia.
摘 要:Various 3,4-dihydropyrimidinones can be prepared via Biginelli reaction in aqueous media by using quaternary ammonium salts of different alkyl groups (C4 and C8) and anions (Cl-?and Br-) as catalysts. The use of quaternary ammonium salts along with longer alkyl chains increases the yield of the Biginelli reaction;however, bromide ammonium salts are less active than the chloride ones.Various 3,4-dihydropyrimidinones can be prepared via Biginelli reaction in aqueous media by using quaternary ammonium salts of different alkyl groups (C4 and C8) and anions (Cl-?and Br-) as catalysts. The use of quaternary ammonium salts along with longer alkyl chains increases the yield of the Biginelli reaction;however, bromide ammonium salts are less active than the chloride ones.
关 键 词:Multicomponent Reaction Biginelli Reaction 3 4-Dihydropyrimidinones Phase-Transfer Catalysis Quaternary Ammonium Salts
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