Comparative Study of Catalytic Potential of TBAB, BTEAC, and CTAB in One-Pot Synthesis of 1,4-Dihydropyridines Under Aqueous Medium
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[1] Cunwei Qian,et al. A clean procedure for the synthesis of 1,4-dihydropyridines via Hantzsch reaction in water , 2013 .
[2] J. Safaei‐Ghomi,et al. CuI Nanoparticles as New, Efficient and Reusable Catalyst for the One-pot Synthesis of 1,4-Dihydropyridines , 2012 .
[3] J. Safaei‐Ghomi,et al. Silica (NPs) supported Fe (III) as a reusable heterogeneous catalyst for the one-pot synthesis of 1, 4-dihydropyridines under mild conditions , 2012, Journal of Chemical Sciences.
[4] H. Behmadi,et al. Polymer Support Immobilized Acidic Ionic Liquid: Preparation and Its Application as Catalyst in the Synthesis of Hantzsch 1,4-Dihydropyridines , 2012 .
[5] M. Gopalakrishnan,et al. An efficient and solvent-free one-pot synthesis of 1,4-dihydropyridines under microwave irradiation , 2011 .
[6] E. Ángeles,et al. Antihypertensive and antiarrhythmic properties of a para-hydroxy[bis(ortho-morpholinylmethyl)]phenyl-1,4-DHP compound: comparison with other compounds of the same kind and relationship with logP values. , 2010, European journal of medicinal chemistry.
[7] K. Sirisha,et al. Facile Synthesis and Antibacterial, Antitubercular, and Anticancer Activities of Novel 1,4‐Dihydropyridines , 2010, Archiv der Pharmazie.
[8] N. Karimi,et al. Brønsted Acid Ionic Liquid [(CH2)4SO3HMIM][HSO4] as Novel Catalyst for One-Pot Synthesis of Hantzsch Polyhydroquinoline Derivatives , 2010 .
[9] Atul Kumar,et al. Synthesis and biological evaluation of N-aryl-1,4-dihydropyridines as novel antidyslipidemic and antioxidant agents. , 2010, European journal of medicinal chemistry.
[10] J. Yadav,et al. CeCl3·7H2O-Catalyzed One-Pot Synthesis of Hantzsch 1,4-Dihydropyridines at Room Temperature , 2009 .
[11] A. Heydari,et al. One-step, synthesis of Hantzsch esters and polyhydroquinoline derivatives in fluoro alcohols , 2009 .
[12] R. Miri,et al. Synthesis and biological evaluation of some new 1,4-dihydropyridines containing different ester substitute and diethyl carbamoyl group as anti-tubercular agents. , 2009, Bioorganic & medicinal chemistry.
[13] S. Fouladdel,et al. Evaluation of anticancer effects of newly synthesized dihydropyridine derivatives in comparison to verapamil and doxorubicin on T47D parental and resistant cell lines in vitro , 2008, Cell Biology and Toxicology.
[14] A. Sudalai,et al. Cu(OTf)2 Catalyzed High Yield Synthesis of Hantzsch 1,4-Dihydropyridines. , 2007 .
[15] Atul Kumar,et al. Synthesis of polyhydroquinoline derivatives through unsymmetric Hantzsch reaction using organocatalysts , 2007 .
[16] M. Zolfigol,et al. Iodine-catalyzed synthesis of novel Hantzsch N-hydroxyethyl 1,4-dihydropyridines under mild conditions , 2007 .
[17] G. Duburs,et al. Distinct effects of atypical 1,4‐dihydropyridines on 1‐methyl‐4‐phenylpyridinium‐induced toxicity , 2007, Cell biochemistry and function.
[18] C. Bruneau,et al. Lewis acid-catalyzed sequential transformations: straightforward preparation of functional dihydropyridines , 2006 .
[19] R. Martín-Aranda,et al. Catalysis by basic carbons: Preparation of dihydropyridines , 2006 .
[20] J. H. Lee. Synthesis of Hantsch 1,4-dihydropyridines by fermenting bakers’ yeast , 2005 .
[21] J. Xia,et al. One-Pot Synthesis and Aromatization of 1,4-Dihydropyridines in Refluxing Water , 2005 .
[22] Murugulla Adharvana Chari,et al. Silica gel/NaHSo4 catalyzed one-pot synthesis of Hantzsch 1,4-dihydropyridines at ambient temperature , 2005 .
[23] H. Tian,et al. Facile Yb(OTf)3 promoted one-pot synthesis of polyhydroquinoline derivatives through Hantzsch reaction , 2005 .
[24] Q. Guo,et al. Synthesis of Substituted 1,4‐Dihydropyridines in Water Using Phase‐Transfer Catalyst Under Microwave Irradiation , 2004 .
[25] J. Yadav,et al. A novel TMSI-mediated synthesis of Hantzsch 1,4-dihydropyridines at ambient temperature , 2003 .
[26] C. Hulme,et al. "Multi-component reactions : emerging chemistry in drug discovery" 'from xylocain to crixivan'. , 2003, Current medicinal chemistry.
[27] P. T. Perumal,et al. SYNTHESIS OF HANTZSCH 1,4-DIHYDROPYRIDINES UNDER MICROWAVE IRRADIATION , 2002 .
[28] J. Yadav,et al. UNPRECEDENTED SYNTHESIS OF HANTZSCH 1,4-DIHYDROPYRIDINES UNDER BIGINELLI REACTION CONDITIONS* , 2001 .
[29] M. Mąkosza. Phase-transfer catalysis. A general green methodology in organic synthesis , 2000 .
[30] A. Hilgeroth,et al. Synthesis and biological evaluation of the first N-alkyl cage dimeric 4-aryl-1,4-dihydropyridines as novel nonpeptidic HIV-1 protease inhibitors. , 1999, Journal of medicinal chemistry.
[31] S. Howlett,et al. Syntheses, calcium channel agonist-antagonist modulation activities, and voltage-clamp studies of isopropyl 1,4-dihydro-2,6-dimethyl-3-nitro-4-pyridinylpyridine-5-carboxylate racemates and enantiomers. , 1995, Journal of medicinal chemistry.
[32] Y. Takahata,et al. Quantitative Structure-Activity Relationships for 1,4-Dihydropyridine Calcium Channel Antagonists (Nifedipine Analogues): A Quantum ChemicalKlassical Approach , 1994 .
[33] J. Serratosa,et al. Anticonvulsant activity of δ-HCH, calcium channel blockers and calmodulin antagonists in seizures induced by lindane and other convulsant drugs , 1993, Brain Research.
[34] Emanuél' Nm,et al. [Geroprotective activity of 2,6-dimethyl-3,5-diethoxycarbonyl-l,4-dihydropyridine]. , 1985 .