A facile protocol for the synthesis of 4-aryl-1,4,7,8-tetrahydro-3,5-dimethyldipyrazolo[3,4-b:4′,3′-e]pyridine derivatives by a Hantzsch-type reaction

[1]  Lei Ma,et al.  An efficient and environmentally friendly procedure for synthesis of pyrimidinone derivatives by use of a Biginelli-type reaction , 2010 .

[2]  Atul Kumar,et al.  Efficient Synthesis of Hantzsch Esters and Polyhydroquinoline Derivatives in Aqueous Micelles , 2008 .

[3]  B. Carboni,et al.  One-Pot Synthesis of 1,4-Dihydropyridines via a Phenylboronic Acid Catalyzed Hantzsch Three-Component Reaction , 2008 .

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

[5]  W. Su,et al.  Europium Triflate–Catalyzed One‐Pot Synthesis of 2,4,5‐Trisubstituted‐1H‐imidazoles via a Three‐component Condensation , 2007 .

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

[7]  M. Zolfigol,et al.  Iodine-catalyzed synthesis of novel Hantzsch N-hydroxyethyl 1,4-dihydropyridines under mild conditions , 2007 .

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

[9]  R. Gibbs,et al.  An efficient one-pot synthesis of polyhydroquinoline derivatives through the Hantzsch four component condensation , 2006 .

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

[11]  B. Hemmateenejad,et al.  Synthesis, study of 3D structures, and pharmacological activities of lipophilic nitroimidazolyl-1,4-dihydropyridines as calcium channel antagonist. , 2006, Bioorganic & medicinal chemistry.

[12]  M. Bagley,et al.  Microwave-Assisted Oxidative Aromatization of Hantzsch 1,4-Dihydro­pyridines using Manganese Dioxide , 2006 .

[13]  Jinlin Li,et al.  Studies on MCM-48 supported cobalt catalyst for Fischer–Tropsch synthesis , 2006 .

[14]  G. Sharma,et al.  'In situ' generated 'HCl' : An efficient catalyst for solvent-free hantzsch reaction at room temperature: Synthesis of new dihydropyridine glycoconjugates , 2006 .

[15]  J. Bazureau,et al.  Ionic liquid phase technology supported the three component synthesis of hantzsch 1,4-dihydropyridines and biginelli 3,4-dihydropyrimidin-2(1H)-ones under microwave dielectric heating , 2005 .

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

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

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

[19]  E. Knaus,et al.  Syntheses, calcium channel agonist-antagonist modulation activities, and nitric oxide release studies of nitrooxyalkyl 1,4-dihydro-2,6-dimethyl-3-nitro-4-(2,1,3-benzoxadiazol-4-yl)pyridine-5-carboxylate racemates, enantiomers, and diastereomers. , 2004, Journal of medicinal chemistry.

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

[21]  P. T. Perumal,et al.  SYNTHESIS OF HANTZSCH 1,4-DIHYDROPYRIDINES UNDER MICROWAVE IRRADIATION , 2002 .

[22]  E. Gordon,et al.  APPROACHES TO COMBINATORIAL SYNTHESIS OF HETEROCYCLES : A SOLID-PHASE SYNTHESIS OF 1,4-DIHYDROPYRIDINES , 1996 .

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

[24]  A M Triggle,et al.  1,4-Dihydropyridine antagonist activities at the calcium channel: a quantitative structure-activity relationship approach. , 1988, Journal of medicinal chemistry.

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

[26]  T. Godfraind,et al.  Calcium antagonism and calcium entry blockade. , 1986, Pharmacological reviews.

[27]  Guengerich Fp,et al.  Oxidation of 4-aryl- and 4-alkyl-substituted 2,6-dimethyl-3,5-bis(alkoxycarbonyl)-1,4-dihydropyridines by human liver microsomes and immunochemical evidence for the involvement of a form of cytochrome P-450. , 1986 .

[28]  D. J. Triggle,et al.  New developments in calcium ion channel antagonists , 1983 .

[29]  D. Stout,et al.  Recent advances in the chemistry of dihydropyridines , 1982 .

[30]  F. Bossert,et al.  4‐Aryldihydropyridines, a New Class of Highly Active Calcium Antagonists , 1981 .

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