Related references
Note: Only part of the references are listed.A highly efficient and green method for the synthesis of 3,4-dihydropyrimidin-2-ones and 1,5-benzodiazepines catalyzed by dodecyl sulfonic acid in water
Saikat Das Sharma et al.
GREEN CHEMISTRY (2007)
Synthesis and differential antiproliferative activity of Biginelli compounds against cancer cell lines:: Monastrol, oxo-monastrol and oxygenated analogues
Dennis Russowsky et al.
BIOORGANIC CHEMISTRY (2006)
Convenient one-pot heterogeneous catalytic method for the preparation of 3,4-dihydropyrimidin-2(1H)-ones
A Hegedus et al.
SYNTHETIC COMMUNICATIONS (2006)
One-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones using boric acid as catalyst
S Tu et al.
TETRAHEDRON LETTERS (2003)
Green chemistry approaches to the synthesis of 5-alkoxycarbonyl-4-aryl-3,4-dihydropyrimidin-2(1H)-ones by a three-component coupling of one-pot condensation reaction:: Comparison of ethanol, water, and solvent-free conditions
DS Bose et al.
JOURNAL OF ORGANIC CHEMISTRY (2003)
Indium(III) bromide-catalyzed preparation of dihydropyrimidinones: improved protocol conditions for the Biginelli reaction
NY Fu et al.
TETRAHEDRON (2002)
N-alkylation of anilines, carboxamides and several nitrogen heterocycles using CsF-celite/alkyl halides/CH3CN combination
S Hayat et al.
TETRAHEDRON (2001)
Indium(III) chloride-catalyzed one-pot synthesis of dihydropyrimidinones by a three-component coupling of 1,3-dicarbonyl compounds, aldehydes, and urea: An improved procedure for the Biginelli reaction
BC Ranu et al.
JOURNAL OF ORGANIC CHEMISTRY (2000)
The guanidine metabolites of Ptilocaulis spiculifer and related compounds; isolation and synthesis
L Heys et al.
CHEMICAL SOCIETY REVIEWS (2000)