A simple approach for the synthesis of dihydropyrimidinones from aldehydes with β-ketoester and urea using BAILs as a catalyst at room temperature and solvent-free condition. This method shows high yields and simple separation techniques. © 2020 Author(s).S. Santra is thankful to the Russian Science Foundation – Russia (Ref. # 18-73-00301) for funding
The majority of the drugs on the market today are entirely chemically synthesized in the laboratory....
The majority of the drugs on the market today are entirely chemically synthesized in the laboratory....
The majority of the drugs on the market today are entirely chemically synthesized in the laboratory....
A simple and efficient method for the one-pot Biginelli condensation reaction of aldehydes, ????-dic...
An efficient synthesis of novel 3,4-dihydropyrimidin-2(1H)-ones (DHPMs) and their derivatives, using...
An efficient and ecofriendly method was developed for synthesis of a series ofdihydropyrimidinone de...
A simple and efficient method for the one-pot Biginelli condensation reaction of aldehydes, -dicarbo...
A general, efficient and green method for the synthesis of dihydropyrimidinones is described under m...
A general, efficient and green method for the synthesis of dihydropyrimidinones is described under m...
A general, efficient and green method for the synthesis of dihydropyrimidinones is described under m...
The ionic liquid catalyst 3-sulfonic acid-1-imidazolopyridinium hydrogen sulfate, [Simp]HSO4 was fou...
AbstractA simple ammonium salt of sulfuric acid in molten state was used as a cheap and mild acidic ...
1378-1384A very simple arrangement of Biginelli’s condensation reaction of 1,3-dicarbonyl compound, ...
677-681Herein is provided an alternate, simple, multigram scale, efficient route for Biginelli react...
The majority of the drugs on the market today are entirely chemically synthesized in the laboratory....
The majority of the drugs on the market today are entirely chemically synthesized in the laboratory....
The majority of the drugs on the market today are entirely chemically synthesized in the laboratory....
The majority of the drugs on the market today are entirely chemically synthesized in the laboratory....
A simple and efficient method for the one-pot Biginelli condensation reaction of aldehydes, ????-dic...
An efficient synthesis of novel 3,4-dihydropyrimidin-2(1H)-ones (DHPMs) and their derivatives, using...
An efficient and ecofriendly method was developed for synthesis of a series ofdihydropyrimidinone de...
A simple and efficient method for the one-pot Biginelli condensation reaction of aldehydes, -dicarbo...
A general, efficient and green method for the synthesis of dihydropyrimidinones is described under m...
A general, efficient and green method for the synthesis of dihydropyrimidinones is described under m...
A general, efficient and green method for the synthesis of dihydropyrimidinones is described under m...
The ionic liquid catalyst 3-sulfonic acid-1-imidazolopyridinium hydrogen sulfate, [Simp]HSO4 was fou...
AbstractA simple ammonium salt of sulfuric acid in molten state was used as a cheap and mild acidic ...
1378-1384A very simple arrangement of Biginelli’s condensation reaction of 1,3-dicarbonyl compound, ...
677-681Herein is provided an alternate, simple, multigram scale, efficient route for Biginelli react...
The majority of the drugs on the market today are entirely chemically synthesized in the laboratory....
The majority of the drugs on the market today are entirely chemically synthesized in the laboratory....
The majority of the drugs on the market today are entirely chemically synthesized in the laboratory....
The majority of the drugs on the market today are entirely chemically synthesized in the laboratory....