A general, efficient and green method for the synthesis of dihydropyrimidinones is described under mild conditions employing low melting mixtures of L-(+)-tartaric acid and urea derivatives as a novel reaction medium. The melt plays a triple role: as solvent, as catalyst and as reactant, furnishing highly functionalized dihydropyrimidinones in good to excellent yields
The majority of the drugs on the market today are entirely chemically synthesized in the laboratory....
A novel domino synthesis of 1,3,5-trisubstituted hydantoin derivatives has been developed in low mel...
A novel domino synthesis of 1,3,5-trisubstituted hydantoin derivatives has been developed in low mel...
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 facile one-pot synthesis of 5-unsubstituted dihydropyrimidinones from β,γ-unsaturated ketoesters i...
A facile one-pot synthesis of 5-unsubstituted dihydropyrimidinones from β,γ-unsaturated ketoesters i...
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...
677-681Herein is provided an alternate, simple, multigram scale, efficient route for Biginelli react...
A simple approach for the synthesis of dihydropyrimidinones from aldehydes with β-ketoester and urea...
Dihydrouracil presents a crucial intermediate in the catabolism of uracil. The vital im-portance of ...
1378-1384A very simple arrangement of Biginelli’s condensation reaction of 1,3-dicarbonyl compound, ...
Synthesis of some 5-acetyl-6-methyl-4-aryl-3,4-dihydropyrimidne-2-one, 5-acetyl-6-methyl-4-aryl-3,4-...
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 novel domino synthesis of 1,3,5-trisubstituted hydantoin derivatives has been developed in low mel...
A novel domino synthesis of 1,3,5-trisubstituted hydantoin derivatives has been developed in low mel...
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 facile one-pot synthesis of 5-unsubstituted dihydropyrimidinones from β,γ-unsaturated ketoesters i...
A facile one-pot synthesis of 5-unsubstituted dihydropyrimidinones from β,γ-unsaturated ketoesters i...
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...
677-681Herein is provided an alternate, simple, multigram scale, efficient route for Biginelli react...
A simple approach for the synthesis of dihydropyrimidinones from aldehydes with β-ketoester and urea...
Dihydrouracil presents a crucial intermediate in the catabolism of uracil. The vital im-portance of ...
1378-1384A very simple arrangement of Biginelli’s condensation reaction of 1,3-dicarbonyl compound, ...
Synthesis of some 5-acetyl-6-methyl-4-aryl-3,4-dihydropyrimidne-2-one, 5-acetyl-6-methyl-4-aryl-3,4-...
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 novel domino synthesis of 1,3,5-trisubstituted hydantoin derivatives has been developed in low mel...
A novel domino synthesis of 1,3,5-trisubstituted hydantoin derivatives has been developed in low mel...