Titanium Dioxide Nanoparticles Catalyzed Synthesis of Hantzsch Esters and Polyhydroquinoline Derivatives

[1]  J. Safari,et al.  Cobalt Nanoparticles Promoted Highly Efficient One Pot Four-Component Synthesis of 1,4-Dihydropyridines under Solvent-Free Conditions , 2011 .

[2]  M. Tajbakhsh,et al.  One-step, synthesis of Hantzsch esters and polyhydroquinoline derivatives using new organocatalyst , 2010 .

[3]  A. Heydari,et al.  A facile and efficient synthesis of β-amino alcohols using 2,2,2-trifluoroethanol as a metal-free and reusable medium , 2010 .

[4]  B. Carboni,et al.  An efficient one-step synthesis of 1,4-dihydropyridines via a triphenylphosphine-catalyzed three-component Hantzsch reaction under mild conditions , 2009 .

[5]  C. Frizzo,et al.  Solvent-free heterocyclic synthesis. , 2009, Chemical reviews.

[6]  A. Heydari,et al.  One-step, synthesis of Hantzsch esters and polyhydroquinoline derivatives in fluoro alcohols , 2009 .

[7]  C. S. Reddy,et al.  Cerium(IV) ammonium nitrate catalysed facile and efficient synthesis of polyhydroquinoline derivatives through Hantzsch multicomponent condensation , 2008 .

[8]  Jinchao Zhang,et al.  The solvent-free synthesis of 1,4-dihydropyridines under ultrasound irradiation without catalyst. , 2008, Ultrasonics sonochemistry.

[9]  Baozhu Tian,et al.  Preparation and characterization of anatase TiO2 microspheres with porous frameworks via controlled hydrolysis of titanium alkoxide followed by hydrothermal treatment , 2008 .

[10]  A. Heydari,et al.  Coupling of Aldehydes, Amines, and Trimethyl Phosphite Promoted by Amberlyst-15: Highly Efficient Synthesis of α-Aminophosphonates , 2008 .

[11]  M. Hundal,et al.  An efficient, catalyst- and solvent-free, four-component, and one-pot synthesis of polyhydroquinolines on grinding , 2008 .

[12]  Atul Kumar,et al.  Synthesis of polyhydroquinoline derivatives through unsymmetric Hantzsch reaction using organocatalysts , 2007 .

[13]  W. Jadhav,et al.  L-Proline as an Efficient Organo-Catalyst for the Synthesis of Polyhydroquinoline Via Multicomponent Hantzsch Reaction , 2007 .

[14]  Y. Tzeng,et al.  A simple and efficient one-pot synthesis of 1,4-dihydropyridines using heterogeneous catalyst under solvent-free conditions , 2006 .

[15]  C. Yao,et al.  Ceric Ammonium Nitrate (CAN) catalyzes the one-pot synthesis of polyhydroquinoline via the Hantzsch reaction , 2006 .

[16]  R. Martín-Aranda,et al.  Catalysis by basic carbons: Preparation of dihydropyridines , 2006 .

[17]  A. Kornienko,et al.  One-step, three-component synthesis of pyridines and 1,4-dihydropyridines with manifold medicinal utility. , 2006, Organic letters.

[18]  A. Shaabani,et al.  Ultrasound-accelerated Synthesis of 1,4-Dihydropyridines in an Ionic Liquid , 2006 .

[19]  J. H. Lee Synthesis of Hantsch 1,4-dihydropyridines by fermenting bakers’ yeast , 2005 .

[20]  Murugulla Adharvana Chari,et al.  Silica gel/NaHSo4 catalyzed one-pot synthesis of Hantzsch 1,4-dihydropyridines at ambient temperature , 2005 .

[21]  C. Yao,et al.  Molecular iodine-catalyzed one-pot synthesis of 4-substituted-1,4-dihydropyridine derivatives via Hantzsch reaction , 2005 .

[22]  Liping Li,et al.  High purity anatase TiO(2) nanocrystals: near room-temperature synthesis, grain growth kinetics, and surface hydration chemistry. , 2005, Journal of the American Chemical Society.

[23]  P. T. Perumal,et al.  A new protocol to synthesize 1,4-dihydropyridines by using 3,4,5-trifluorobenzeneboronic acid as a catalyst in ionic liquid: synthesis of novel 4-(3-carboxyl-1H-pyrazol-4-yl)-1,4-dihydropyridines , 2005 .

[24]  A. Agarwal,et al.  Solid supported synthesis of structurally diverse dihydropyrido[2,3-d]pyrimidines using microwave irradiation , 2005 .

[25]  H. Tian,et al.  Facile Yb(OTf)3 promoted one-pot synthesis of polyhydroquinoline derivatives through Hantzsch reaction , 2005 .

[26]  T. Loh,et al.  Facile Ionic Liquids-Promoted One-Pot Synthesis of Polyhydroquinoline Derivatives under Solvent Free Conditions , 2004 .

[27]  V. Bertolasi,et al.  Multicomponent Hantzsch cyclocondensation as a route to highly functionalized 2- and 4-dihydropyridylalanines, 2- and 4-pyridylalanines, and their N-oxides: preparation via a polymer-assisted solution-phase approach , 2004 .

[28]  S. Sabbatini,et al.  Model studies toward the synthesis of dihydropyrimidinyl and pyridyl alpha-amino acids via three-component Biginelli and Hantzsch cyclocondensations. , 2003, The Journal of organic chemistry.

[29]  J. Yadav,et al.  A novel TMSI-mediated synthesis of Hantzsch 1,4-dihydropyridines at ambient temperature , 2003 .

[30]  I. Chen,et al.  The new generation dihydropyridine type calcium blockers, bearing 4-phenyl oxypropanolamine, display α-/β-Adrenoceptor antagonist and long-Acting antihypertensive activities , 2002 .

[31]  A. Shafiee,et al.  Synthesis and calcium channel antagonist activities of 3-nitrooxyalkyl, 5-alkyl 1,4-dihydro-2,6-dimethyl-4-(1-methyl-5-nitro-2-imidazolyl)-3, 5-pyridinedicarboxylates. , 2002, Farmaco.

[32]  J. Westman,et al.  An Efficient and Fast Procedure for the Hantzsch Dihydropyridine Synthesis under Microwave Conditions , 2001 .

[33]  J. Breitenbucher,et al.  Solid-phase synthesis of 4-aryl-1,4-dihydropyridines via the Hantzsch three component condensation , 2000 .

[34]  S. S. Chimni,et al.  Acid catalysed enamine induced transformations of 1,3-dimethyl-5-formyluracil. A unique annulation reaction with enaminones , 1995 .

[35]  B. M. Khadilkar,et al.  AQUEOUS HYDROTROPE SOLUTION AS A SAFER MEDIUM FOR MICROWAVE ENHANCED HANTZSCH DIHYDROPYRIDINE ESTER SYNTHESIS , 1995 .

[36]  J. V. Eynde,et al.  Old reagents, new results: Aromatization of Hantzsch 1,4-dihydropyridines with manganese dioxide and 2,3-dichloro-5,6-dicyano-1,4-benzoquinone , 1995 .

[37]  R. Mannhold,et al.  Calcium- and calmodulin-antagonism of elnadipine derivatives: comparative SAR , 1992 .

[38]  G. Duburs,et al.  Synthesis of 1,4-dihydropyridines by cyclocondensation reactions , 1988 .

[39]  G. Berkelhammer,et al.  A Study of the Primary Acid Reaction on Model Compounds of Reduced Diphosphopyridine Nucleotide1,2 , 1958 .

[40]  A. P. Phillips Hantzsch's Pyridine Synthesis , 1949 .

[41]  A. Hantzsch Ueber die Synthese pyridinartiger Verbindungen aus Acetessigäther und Aldehydammoniak , 1882 .