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
暂无分享,去创建一个
[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 .