Synthesis and characterization of functionalized dihydropyrimidinones via one-pot isocyanide-based three-component reaction of N-formyl urea and dialkyl ACETYLENEDICARBOXYLATES
暂无分享,去创建一个
[1] A. Ramazani,et al. Silica nanoparticles as a highly efficient catalyst for the one-pot synthesis of sterically congested 2-(dibenzylamino)-2-aryl acetamide derivatives from by phthaldehyde isomers, isocyanides and dibenzylamine , 2017 .
[2] I. V. Omelchenko,et al. One-pot synthesis of new derivatives of 3,4-dihydropyrimidinone, and substituted imidazolin-2-ones , 2015 .
[3] Mohammad Moradi. Benzyltriphenylphosphonium Chloride: A Efficient Catalyst for One-Pot Synthesis of Dihydropyrimidinones/Thiones under Solvent-Free Conditions , 2015 .
[4] R. Nongrum,et al. One-pot Synthesis of 3,4-Dihydropyrimidin-2(1H)-ones Catalysed by Cupric Acetate under Solvent-free Conditions , 2014 .
[5] Xufeng Lin,et al. Efficient synthesis of dihydropyrimidinones via a three-component Biginelli-type reaction of urea, alkylaldehyde and arylaldehyde , 2013, Beilstein journal of organic chemistry.
[6] H. Abdel-ghany,et al. Eco-Friendly Synthesis of Pyrimidine and Dihydropyrimidinone Derivatives under Solvent Free Condition and their Anti-microbial Activity , 2013 .
[7] A. Chakraborti,et al. Organocatalytic Application of Ionic Liquids: [bmim][MeSO4] as a Recyclable Organocatalyst in the Multicomponent Reaction for the Preparation of Dihydropyrimidinones and ‐thiones. , 2011 .
[8] T. Müller. Multicomponent reactions , 2011, Beilstein journal of organic chemistry.
[9] K. Pandiarajan,et al. Synthesis and in vitro microbiological evaluation of novel 4-aryl-5-isopropoxycarbonyl-6-methyl-3,4-dihydropyrimidinones. , 2010, European journal of medicinal chemistry.
[10] M. Heravi,et al. EFFICIENT SODIUM SELENATE-CATALYZED SYNTHESIS OF 3,4-DIHYDRO-2(1 H )-PYRIMIDINONES AND –THIONES UNDER SOLVENT-FREE CONDITIONS , 2009 .
[11] Xiao‐hong Wang,et al. A Green Synthesis of Dihydropyrimidinones by Biginelli Reaction over Nafion‐H Catalyst. , 2008 .
[12] M. P. Kaushik,et al. Synthesis of 4-aryl substituted 3,4-dihydropyrimidinones using silica-chloride under solvent free conditions. , 2007, Molecules.
[13] D. Tejedor,et al. Chemo-Differentiating ABB′ Multicomponent Reactions: Privileged Building Blocks , 2007 .
[14] R. Dabur,et al. Microwave-assisted synthesis of antimicrobial dihydropyridines and tetrahydropyrimidin-2-ones: novel compounds against aspergillosis. , 2006, Bioorganic & medicinal chemistry.
[15] Alexander Dömling,et al. Recent developments in isocyanide based multicomponent reactions in applied chemistry. , 2006, Chemical reviews.
[16] Fan Xu,et al. An Efficient One-Pot Synthesis of Dihydropyrimidinones by a Samarium Diiodide Catalyzed Biginelli Reaction under Solvent-Free Conditions. , 2005 .
[17] Jieping Zhu,et al. Multicomponent Reactions: ZHU:MULTICOMPONENT REACTIONS O-BK , 2005 .
[18] A. Doemling,et al. The Chemistry of Isocyanides, Their Multicomponent Reactions and Their Libraries , 2004 .
[19] B. Trost,et al. On inventing reactions for atom economy. , 2002, Accounts of chemical research.
[20] C. Kappe. Biologically active dihydropyrimidones of the Biginelli-type--a literature survey. , 2000, European journal of medicinal chemistry.
[21] T. Torroba,et al. The Use of Isocyanides in Heterocyclic 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] I. Ugi. From Isocyanides via Four-Component Condensations to Antibiotic Syntheses†‡ , 1982 .