Microwave-assisted synthesis of dihydropyrimidin-2(1H)-ones using graphite supported lanthanum chloride as a mild and efficient catalyst.
暂无分享,去创建一个
[1] X. Hui,et al. A Rapid and Efficient Biginelli Reaction Catalyzed by Zinc Triflate , 2010 .
[2] H. Hazarkhani,et al. Trichloroisocyanuric acid, a new and efficient catalyst for the synthesis of dihydropyrimidinones , 2007 .
[3] K. Saidi,et al. Solvent free microwave assisted Doebner reaction: A green method for the preparation of cinnamic acids , 2007 .
[4] B. Bhanage,et al. Y(NO3)3·6H2O: A novel and reusable catalyst for one pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones under solvent-free conditions , 2007 .
[5] Yang Yu,et al. One-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones using chloroacetic acid as catalyst. , 2007, Bioorganic & medicinal chemistry letters.
[6] F. Shirini,et al. Silica triflate as an efficient catalyst for the solvent-free synthesis of 3,4-dihydropyrimidin-2(1H)-ones , 2007 .
[7] M. G. D’Oca,et al. Multicomponent Biginelli's synthesis of 3,4-dihydropyrimidin-2(1H)-ones promoted by SnCl2.2H2O , 2004 .
[8] A. Katritzky,et al. Microwave-assisted heterocyclic synthesis , 2003 .
[9] A. Sudalai,et al. Cu(OTf)2: a reusable catalyst for high-yield synthesis of 3,4-dihydropyrimidin-2(1H)-ones , 2003 .
[10] A. Shaabani,et al. Ammonium chloride-catalyzed one-pot synthesis of 3,4-dihydropyrimidin-2-(1H)-ones under solvent-free conditions , 2003 .
[11] H. Tian,et al. Lanthanide Triflate Catalyzed One-Pot Synthesis of Dihydropyrimidin-2(1H)-thiones by a Three-Component of 1,3-Dicarbonyl Compounds, Aldehydes, and Thiourea Using a Solvent-Free Biginelli Condensation , 2003 .
[12] Shan-Wei Wang,et al. Indium(III) bromide-catalyzed preparation of dihydropyrimidinones: improved protocol conditions for the Biginelli reaction , 2002 .
[13] K. Ramalinga,et al. Bismuth(III)-Catalyzed Synthesis of Dihydropyrimidinones: Improved Protocol Conditions for the Biginelli Reaction , 2001 .
[14] C. Kappe. Biologically active dihydropyrimidones of the Biginelli-type--a literature survey. , 2000, European journal of medicinal chemistry.
[15] Jun Lu,et al. One-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones using lanthanum chloride as a catalyst , 2000 .
[16] C. Kappe. Recent advances in the Biginelli dihydropyrimidine synthesis. New tricks from an old dog. , 2000, Accounts of chemical research.
[17] E. Hu,et al. Unprecedented Catalytic Three Component One-Pot Condensation Reaction: An Efficient Synthesis of 5-Alkoxycarbonyl- 4-aryl-3,4-dihydropyrimidin-2(1H)-ones , 1998 .
[18] C. Kappe,et al. Conformational analysis of 4-aryl-dihydropyrimidine calcium channel modulators. A comparison of ab initio, semiempirical and X-ray crystallographic studies , 1997 .
[19] Jinsheng Chen,et al. Synthesis of the tricyclic portions of batzelladines A, B and D. Revision of the stereochemistry of batzelladines A and D , 1996 .
[20] Rongan Zhang,et al. Calcium entry blockers and activators: conformational and structural determinants of dihydropyrimidine calcium channel modulators. , 1995, Journal of medicinal chemistry.
[21] C. Kappe. 100 years of the biginelli dihydropyrimidine synthesis , 1993 .
[22] A Hedberg,et al. Dihydropyrimidine calcium channel blockers. 3. 3-Carbamoyl-4-aryl-1,2,3,4-tetrahydro-6-methyl-5-pyrimidinecarboxylic acid esters as orally effective antihypertensive agents. , 1991, Journal of medicinal chemistry.
[23] A. Ballesteros,et al. 1,4-Cycloaddition of 1,3-diazabutadienes with enamines: an efficient route to the pyrimidine ring , 1989 .
[24] K. Atwal,et al. Synthesis of substituted 1,2,3,4-tetrahydro-6-methyl-2-oxo-5-pyrimidinecarboxylic acid esters: the Biginelli condensation revisited , 1987 .