3-[(3-(Trimethoxysilyl)propyl)thio]propane-1-oxy-sulfonic acid: An efficient recyclable heterogeneous catalyst for the synthesis of 3,4-dihydropyrimidin-2(1H)-ones/thiones
暂无分享,去创建一个
[1] A. Hajipour,et al. Pyridinium-Based Brønsted Acidic Ionic Liquid as a Highly Efficient Catalyst for One-Pot Synthesis of Dihydropyrimidinones , 2012 .
[2] L. Gong,et al. Brønsted-acid-catalyzed asymmetric multicomponent reactions for the facile synthesis of highly enantioenriched structurally diverse nitrogenous heterocycles. , 2011, Accounts of chemical research.
[3] Meimei Xu,et al. Edaxadiene: A New Bioactive Diterpene from Mycobacterium tuberculosis , 2010, Journal of the American Chemical Society.
[4] Nitin P. Lad,et al. Recyclable Amberlyst-70 as a Catalyst for Biginelli Reaction: An Efficient One-Pot Green Protocol for the Synthesis of 3,4-Dihydropyrimidin-2(1H)-ones , 2009 .
[5] F. Behbahani,et al. Ferric Perchlorate Catalyzed One-pot Synthesis of 1,2,3,4-Tetrahydro-2-pyrimidinones and -thiones: an Expedient Protocol for the Biginelli Reaction , 2008 .
[6] M. P. Kaushik,et al. Synthesis of 4-aryl substituted 3,4-dihydropyrimidinones using silica-chloride under solvent free conditions. , 2007, Molecules.
[7] S. Kantevari,et al. HClO4–SiO2 and PPA–SiO2 catalyzed efficient one-pot Knoevenagel condensation, Michael addition and cyclo-dehydration of dimedone and aldehydes in acetonitrile, aqueous and solvent free conditions: Scope and limitations , 2007 .
[8] M. Krishnaiah,et al. Sulfonic acid functionalized silica : A remarkably efficient heterogeneous reusable catalyst for α-monobromination of carbonyl compounds using N-bromosuccinimide , 2006 .
[9] A. Hajipour,et al. Nitric acid in the presence of P2O5 supported on silica gel—a useful reagent for nitration of aromatic compounds under solvent-free conditions , 2005 .
[10] W. Su,et al. One-pot synthesis of dihydropyrimidiones catalyzed by strontium(II) triflate under solvent-free conditions , 2005 .
[11] A. Chakraborty,et al. In(OTf)3-catalysed one-pot synthesis of 3,4-dihydropyrimidin-2(lH)-ones , 2004 .
[12] V. Choudhary,et al. Microwave assisted solvent-free synthesis of dihydropyrimidinones by Biginelli reaction over Si-MCM-41 supported FeCl3 catalyst , 2003 .
[13] M. Zolfigol,et al. Silica sulfuric acid: an efficient and reusable catalyst for the one-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones , 2003 .
[14] A. Shaabani,et al. Ammonium chloride-catalyzed one-pot synthesis of 3,4-dihydropyrimidin-2-(1H)-ones under solvent-free conditions , 2003 .
[15] M. Mahesh,et al. Zirconium(IV) chloride catalyzed one-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones☆ , 2002 .
[16] K. Raghavan,et al. Zeolite-catalyzed cyclocondensation reaction for the selective synthesis of 3,4-dihydropyrimidin-2(1H)-ones , 2001 .
[17] 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 .
[18] J. Yadav,et al. Ultrasound-accelerated synthesis of 3,4-dihydropyrimidin-2(1H)-ones with ceric ammonium nitrate , 2001 .
[19] C. Kappe. Recent advances in the Biginelli dihydropyrimidine synthesis. New tricks from an old dog. , 2000, Accounts of chemical research.
[20] B. Ranu,et al. 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. , 2000, The Journal of organic chemistry.
[21] C. Kappe,et al. Biginelli condensations of fluorinated 3-oxo esters and 1,3-diketones , 2000 .
[22] R. Chang,et al. Design and synthesis of novel alpha(1)(a) adrenoceptor-selective antagonists. 1. Structure-activity relationship in dihydropyrimidinones. , 1999, Journal of medicinal chemistry.
[23] S. Carloni,et al. A revision of the Biginelli reaction under solid acid catalysis. Solvent-free synthesis of dihydropyrimidines over montmorillonite KSF , 1999 .
[24] C. Kappe,et al. Polyphosphate Ester-Mediated Synthesis of Dihydropyrimidines. Improved Conditions for the Biginelli Reaction , 1998 .
[25] 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 .
[26] 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 .
[27] 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 .
[28] M. F. Bean,et al. Novel Alkaloids from the Sponge Batzella sp.: Inhibitors of HIV gp120-Human CD4 Binding , 1995 .
[29] C. Kappe. 100 years of the biginelli dihydropyrimidine synthesis , 1993 .