In this study, a novel, clean, convenient, appropriate and environmentally benign route to dihydropyrimidinone and thione derivatives has been developed using the reaction between various benzaldehydes, urea or thiourea, and ethyl acetoacetate in the presence of Fe+3-montmorillonite K10 under grind condition. The present methodology has several advantages such as simple work-up, solvent-free conditions, environmental friendliness and shorter reaction time along with high yields. Several aromatic aldehydes carrying either electron-releasing or electron-withdrawing substituents in the ortho and para positions were tested in this reaction. Another important feature of this procedure is the survival of a variety of functional groups under the r...
Aldehydes were cleanly and selectively converted to the corresponding dithioacetals almost quantitat...
AbstractAn efficient method for the synthesis of 3,4-dihydropyrimidin-2(1H)-ones and thiones through...
Facile and environment-friendly procedure for the synthesis of corresponding 3,4-dihydropyrimidin-2-...
Copyright © 2013 A. M. Elmaghraby et al. This is an open access article distributed under the Creati...
The Mg/Fe = 3 hydrotalcite as reusable solid catalyst was found to be an excellent heterogeneous bas...
AbstractObjectivesThis paper aims to describe the synthesis of a series of novel 5-substituted dihyd...
160-164An efficient synthesis of Biginelli-type compounds using maleic acid as an economical di-func...
International audienceIn this work, we report a simple, efficient and green protocol for the synthes...
The majority of the drugs on the market today are entirely chemically synthesized in the laboratory....
A simple, green and efficient solventless procedure for the synthesis of 3,4-dihydropyrimidin-2-(1H)...
Montmorillonite clays are reported as efficient, inexpensive, and reusable catalysts for carbon–sulf...
An environmental friendly, economical and clean Biginelli approach in presence of readily available ...
An efficient and direct procedure for the synthesis of 4,6-diphenyl-3,4-dihydropyrimidine-2(1H)-thio...
A sustainable, green one-pot process for the synthesis of dihydropyrimidinones (DHPMs) derivatives b...
In this study, we present a simple, economical and environmentally friendly approach to synthesize 3...
Aldehydes were cleanly and selectively converted to the corresponding dithioacetals almost quantitat...
AbstractAn efficient method for the synthesis of 3,4-dihydropyrimidin-2(1H)-ones and thiones through...
Facile and environment-friendly procedure for the synthesis of corresponding 3,4-dihydropyrimidin-2-...
Copyright © 2013 A. M. Elmaghraby et al. This is an open access article distributed under the Creati...
The Mg/Fe = 3 hydrotalcite as reusable solid catalyst was found to be an excellent heterogeneous bas...
AbstractObjectivesThis paper aims to describe the synthesis of a series of novel 5-substituted dihyd...
160-164An efficient synthesis of Biginelli-type compounds using maleic acid as an economical di-func...
International audienceIn this work, we report a simple, efficient and green protocol for the synthes...
The majority of the drugs on the market today are entirely chemically synthesized in the laboratory....
A simple, green and efficient solventless procedure for the synthesis of 3,4-dihydropyrimidin-2-(1H)...
Montmorillonite clays are reported as efficient, inexpensive, and reusable catalysts for carbon–sulf...
An environmental friendly, economical and clean Biginelli approach in presence of readily available ...
An efficient and direct procedure for the synthesis of 4,6-diphenyl-3,4-dihydropyrimidine-2(1H)-thio...
A sustainable, green one-pot process for the synthesis of dihydropyrimidinones (DHPMs) derivatives b...
In this study, we present a simple, economical and environmentally friendly approach to synthesize 3...
Aldehydes were cleanly and selectively converted to the corresponding dithioacetals almost quantitat...
AbstractAn efficient method for the synthesis of 3,4-dihydropyrimidin-2(1H)-ones and thiones through...
Facile and environment-friendly procedure for the synthesis of corresponding 3,4-dihydropyrimidin-2-...