819
Views
19
CrossRef citations to date
0
Altmetric
Original Article

An efficient one-pot synthesis of 1,4-dihydropyridine derivatives through Hantzsch reaction catalysed by melamine trisulfonic acidFootnote

Pages 1-9 | Received 07 Nov 2012, Accepted 16 Dec 2012, Published online: 16 Apr 2018

References

  • A.DomlingI.UgiMulticomponent reactions with isocyanidesAngewandte Chemie International Edition39200031683210
  • A.HantzschUeber die synthese pyridinartiger verbindungen aus acetessigather und aldehydammoniakJustus Liebigs Annalen der Chemie2151882182
  • T.TsuruoH.IidaM.NojiriS.TsukagoshiY.SakuraiCircumvention of vincristine and adriamycin resistance in vitro and in vivo by calcium influx blockersCancer Research43198329052910
  • A.KrauzeS.GermaneO.EberlinsI.SturmsV.KlusaG.DubursDerivatives of 3-cyano-6-phenyl-4-(3′-pyridyl)pyridine-2(1H)-thione and their neurotropic activityEuropean Journal of Medicinal Chemistry341999301310
  • X.ZhouL.ZhangE.TsengE.Scott-RamsayJ.J.SchentagR.A.CoburnM.E.MorrisNew 4-aryl-1,4-dihydropyridines and 4-arylpyridines as P-glycoprotein inhibitorsDrug Metabolism and Disposition332005321328
  • R.W.ChapmanG.DankoM.I.SiegelsEffect of extra- and intracellular calcium blockers on histamine and antigen-induced bronchospasm in guinea pigs and ratsPharmacology291984282291
  • W.J.MalaiseP.C.F.MathiasStimulation of insulin release by organic calcium-agonistDiabetologia281985153156
  • A.R.TrivediD.K.DodiyaB.H.DholariyaV.B.KatariaV.R.BhuvaV.H.ShahSynthesis and biological evaluation of some novel N-aryl-1,4-dihydropyridines as potential antitubercular agentsBioorganic & Medicinal Chemistry Letters21201151815183
  • M.KhoshneviszadehN.EdrakiK.JavidniaA.AlborziB.PourabbasJ.MardanehR.MirSynthesis and biological evaluation of some new 1,4-dihydropyridines containing different ester substitute and diethyl carbamoyl group as anti-tubercular agentsBioorganic & Medicinal Chemistry17200915791586
  • M.M.HeraviK.BakhtiriN.M.JavadiF.F.BamoharramM.SaeediH.A.OskooiK7[PW11CoO40]-catalyzed one-pot synthesis of polyhydroquinoline derivatives via the Hantzsch three component condensationJournal of Molecular Catalysis A: Chemical26420075052
  • S.R.CherkupallyR.Mekalanp-TSA catalyzed facile and efficient synthesis of polyhydroquinoline derivatives through Hantzsch multi-component condensationChemical and Pharmaceutical Bulletin56200810021004
  • S.KumarP.SharmaK.K.KapoorM.S.HundalAn efficient, catalyst- and solvent-free, four-component, and one-pot synthesis of polyhydroquinolines on grindingTetrahedron642008536542
  • R.SurasaniD.KalitaA.V.D.RaoK.YarbagiK.B.ChandrasekharFeF3 as a novel catalyst for the synthesis of polyhydroquinoline derivatives via unsymmetrical Hantzsch reactionJournal of Fluorine Chemistry13520129196
  • L.M.WangJ.ShengL.ZhangJ.W.HanZ.FanH.TianC.T.QianFacile Yb(OTf)3 promoted one-pot synthesis of polyhydroquinoline derivatives through Hantzsch reactionTetrahedron61200515391543
  • M.MaheswaraV.SiddaiahG.L.V.DamuC.V.RaoAn efficient one-pot synthesis of polyhydroquinoline derivatives via Hantzsch condensation using a heterogeneous catalyst under solvent-free conditionsARKIVOC22006201206
  • J.SafariS.H.BanitabaS.D.KhaliliCellulose sulfuric acid catalyzed multicomponent reaction for efficient synthesis of 1,4-dihydropyridines via unsymmetrical Hantzsch reaction in aqueous mediaJournal of Molecular Catalysis A: Chemical33520114650
  • A.DebacheW.GhalemR.BoulcinaA.BelfaitahS.RhouatiB.CarboniAn efficient one-step synthesis of 1,4-dihydropyridines via a triphenylphosphine-catalyzed three-component Hantzsch reaction under mild conditionsTetrahedron Letters50200952485250
  • N.N.KaradeV.H.BudhewarS.V.ShindeW.N.JadhavL-Proline as an efficient organo catalyst for the synthesis of polyhydroquinoline via multicomponent Hantzsch reactionLetters in Organic Chemistry420071619
  • J.AlbadiF.ShiriniB.GhabeziT.SeiadatnasabMelamine trisulfonic acid catalyzed regioselevtive nitration of aromatic compounds with sodium nitrate under solvent-free conditionsArabian Journal of Chemistry201210.1016/j.arabjc.2012.10.011
  • X.J.YangY.S.ZhangMelamine trisulfonic acid-catalyzed N-formylation of amines under solvent-free conditionsResearch on Chemical Intermediates201210.1007/s11164-012-0803-7
  • L.WuY.YanF.YanMelamine trisulfonic acid: a new efficient catalyst for the synthesis of aryldithienylmethanesPhosphorus, Sulfur, and Silicon and the Related Elements18722012149154
  • L.YangP.SunL.WuOne-pot three-component synthesis of spiro[pyrazolo[3,4-b]pyridine-4,3′-indoline] derivatives catalyzed by melamine trisulfonic acidJournal of the Chinese Chemical Society201210.1002/jccs.201200046
  • S.S.MansoorS.S.ShafiS.Z.AhmedAn efficient one-pot multicomponent synthesis of 3,4-dihydropyrimidine-2-(1H)-ones/thiones/imines via a Lewis base catalyzed Biginelli-type reaction under solvent-free conditionsArabian Journal of Chemistry201110.1016/j.arabjc.2011.09.018
  • S.S.MansoorK.AswinK.LogaiyaS.P.N.SudhanAn efficient synthesis of β-amino ketone compounds through one-pot three-component Mannich-type reactions using bismuth nitrate as catalystJournal of Saudi Chemical Society201210.1016/j.jscs.2012.04.008
  • S.S.MansoorK.AswinK.LogaiyaS.P.N.SudhanZrOCl2.8H2O: an efficient and recyclable catalyst for the three-component synthesis of amidoalkyl naphthols under solvent-free conditionsJournal of Saudi Chemical Society201210.1016/j.jscs.2012.06.003
  • S.S.MansoorK.AswinK.LogaiyaS.P.N.Sudhan[Bmim]BF4 ionic liquid: an efficient reaction medium for the one-pot multi-component synthesis of 2-amino-4,6-diphenylpyridine-3-carbonitrile derivativesJournal of Saudi Chemical Society201210.1016/j.jscs.2012.07.011
  • S.S.MansoorK.AswinK.LogaiyaS.P.N.SudhanAn efficient one-pot three-component synthesis of α-amino nitriles via Strecker reaction catalysed by bismuth(III) nitrateJournal of Saudi Chemical Society201210.1016/j.jscs.2012.10.009
  • F.ShiriniM.A.ZolfigolJ.AlbadiMelamine trisulfonic acid as a new, efficient and reusable catalyst for the solvent free synthesis of coumarinsJournal of the Iranian Chemical Society742010895899

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.