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

[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 .