New three-component cyclocondensation reaction: microwave-assisted one-pot synthesis of 5-unsubstituted-3,4-dihydropyrimidin-2(1H)-ones under solvent-free conditions

[1]  C. Kappe,et al.  Microwave-enhanced and metal-catalyzed functionalizations of the 4-aryl-dihydropyrimidone template. , 2005, Journal of combinatorial chemistry.

[2]  C. Kappe,et al.  Microwave-assisted multistep synthesis of functionalized 4-arylquinolin-2(1H)-ones using palladium-catalyzed cross-coupling chemistry. , 2005, Journal of Organic Chemistry.

[3]  Ira Saxena,et al.  Three component condensations catalyzed by iodine-alumina for the synthesis of substituted 3,4-dihydropyrimidin-2(1H)-ones under microwave irradiation and solvent-free conditions , 2005 .

[4]  C. Xia,et al.  Novel Biginelli-like three-component cyclocondensation reaction: efficient synthesis of 5-unsubstituted 3,4-dihydropyrimidin-2(1H)-ones , 2004 .

[5]  C. Kappe,et al.  Tunable carbon-carbon and carbon-sulfur cross-coupling of boronic acids with 3,4-dihydropyrimidine-2-thiones. , 2004, Organic letters.

[6]  O. Lavastre,et al.  Microwave-assisted ring-closing metathesis revisited. On the question of the nonthermal microwave effect. , 2003, The Journal of organic chemistry.

[7]  Shan-Wei Wang,et al.  Indium(III) bromide-catalyzed preparation of dihydropyrimidinones: improved protocol conditions for the Biginelli reaction , 2002 .

[8]  M. Mahesh,et al.  Zirconium(IV) chloride catalyzed one-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones☆ , 2002 .

[9]  Pei-jun Cai,et al.  A CONVENIENT FERRIC CHLORIDE CATALYZED SYNTHESIS OF 5-ALKOXYCARBONYL-4-ARYL-3,4-DIHYDROPYRIMIDIN-2(1H)-ONES UNDER MICROWAVE IRRADIATION , 2002 .

[10]  A. Dondoni,et al.  Parallel synthesis of dihydropyrimidinones using Yb(III)-resin and polymer-supported scavengers under solvent-free conditions. A green chemistry approach to the Biginelli reaction , 2001 .

[11]  K. Ramalinga,et al.  Bismuth(III)-Catalyzed Synthesis of Dihydropyrimidinones: Improved Protocol Conditions for the Biginelli Reaction , 2001 .

[12]  J. Yadav,et al.  Ultrasound-accelerated synthesis of 3,4-dihydropyrimidin-2(1H)-ones with ceric ammonium nitrate , 2001 .

[13]  C. Kappe.  Biologically active dihydropyrimidones of the Biginelli-type--a literature survey. , 2000, European journal of medicinal chemistry.

[14]  C. Qian,et al.  Lanthanide triflate catalyzed Biginelli reaction. one-pot synthesis of dihydropyrimidinones under solvent-free conditions. , 2000, The Journal of organic chemistry.

[15]  C. Kappe,et al.  X-Ray Structure, Conformational Analysis, Enantioseparation, and Determination of Absolute Configuration of the Mitotic Kinesin Eg5 Inhibitor Monastrol , 2000 .

[16]  Rajender S. Varma,et al.  Microwave-Assisted High-Speed Parallel Synthesis of 4-Aryl-3,4-dihydropyrimidin-2(1H)-ones using a Solventless Biginelli Condensation Protocol , 1999 .

[17]  Zhengyin Du,et al.  The Synthesis of 1,3-bis(Phenylseleno)-2-Propanol Under Microwave Irradiation Conditions , 1998 .

[18]  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 .

[19]  M. F. Bean,et al.  Novel Alkaloids from the Sponge Batzella sp.: Inhibitors of HIV gp120-Human CD4 Binding , 1995 .

[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]  S. Moreland,et al.  Dihydropyrimidine calcium channel blockers. 4. Basic 3-substituted-4-aryl-1,4-dihydropyrimidine-5-carboxylic acid esters. Potent antihypertensive agents. , 1992, Journal of medicinal chemistry.

[23]  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.