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Volumn 15, Issue 9, 2011, Pages 1423-1463

Recent advances in the chemistry of pyrazoles. properties, biological activities, and syntheses

Author keywords

1,3 dipolar cycloaddition; Condensation; Diazo compounds; Hydrazines; N heterocyclic carbene; Natural products; Rearrangement; Regiochemistry

Indexed keywords

NITROGEN COMPOUNDS; ORGANIC COMPOUNDS;

EID: 79958200235     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/138527211795378263     Document Type: Review
Times cited : (304)

References (276)
  • 1
    • 0011235592 scopus 로고    scopus 로고
    • R. Neier, Ed.; Thieme Verlag: Stuttgart
    • Stanovnik, B.; Svete, J. In: Science of Synthesis, R. Neier, Ed.; Thieme Verlag: Stuttgart, 2002; Vol. 12, pp. 15-225.
    • (2002) Science of Synthesis , vol.12 , pp. 15-225
    • Stanovnik, B.1    Svete, J.2
  • 3
    • 0000756640 scopus 로고
    • D. H. R. Barton, W. D. Ollis, Eds.; Pergamon: Oxford
    • Grimmett, M.R. In: Comprehensive Organic Chemistry, D. H. R. Barton, W. D. Ollis, Eds.; Pergamon: Oxford, 1979, 4, 357-410.
    • (1979) Comprehensive Organic Chemistry , vol.4 , pp. 357-410
    • Grimmett, M.R.1
  • 4
    • 0004246795 scopus 로고
    • R. C. Elderfield, Ed.; Wiley: New York
    • Jacobs, T.L. In: Heterocyclic Compounds, R. C. Elderfield, Ed.; Wiley: New York 1957, 5, 45-162.
    • (1957) Heterocyclic Compounds , vol.5 , pp. 45-162
    • Jacobs, T.L.1
  • 7
    • 84943407995 scopus 로고
    • A. R. Katritzky, C. W. Rees, Eds.; Pergamon: Oxford
    • Elguero, J. In: Comprehensive Heterocyclic Chemistry, A. R. Katritzky, C. W. Rees, Eds.; Pergamon: Oxford 1984, vol. 5, pp. 167-303.
    • (1984) Comprehensive Heterocyclic Chemistry , vol.5 , pp. 167-303
    • Elguero, J.1
  • 8
    • 84944033746 scopus 로고    scopus 로고
    • A. R. Katritzky, E. F. V. Scriven, Eds.; Elsevier: Oxford
    • Elguero, J. In: Comprehensive Heterocyclic Chemistry II, A. R. Katritzky, E. F. V. Scriven, Eds.; Elsevier: Oxford 1996, vol. 3, pp. 1-75.
    • (1996) Comprehensive Heterocyclic Chemistry II , vol.3 , pp. 1-75
    • Elguero, J.1
  • 9
    • 0032950304 scopus 로고    scopus 로고
    • Synthesis of pyrazoles and condensed pyrazoles
    • Makino, K.; Kim, H.S.; Kurasawa, Y. Synthesis of pyrazoles and condensed pyrazoles. J. Heterocycl. Chem., 1999, 36(2), 321-332.
    • (1999) J. Heterocycl. Chem , vol.36 , Issue.2 , pp. 321-332
    • Makino, K.1    Kim, H.S.2    Kurasawa, Y.3
  • 11
    • 0029819305 scopus 로고    scopus 로고
    • Ring transformation of 5-acylpyrimidines and 5-acyluracils into pyrazoles with hydrazines in acidic medium
    • Takagi, K.; Hubert-Habart, M. Ring transformation of 5-acylpyrimidines and 5-acyluracils into pyrazoles with hydrazines in acidic medium. J. Heterocycl. Chem., 1996, 33(4),1003-1015.
    • (1996) J. Heterocycl. Chem , vol.33 , Issue.4 , pp. 1003-1015
    • Takagi, K.1    Hubert-Habart, M.2
  • 12
    • 84948499677 scopus 로고
    • Recent developments in the synthesis of pyrazole derivatives
    • Elnagdi, M.H.; Elgemeie, G.E.H.; Abd-Elaal, F. A.-E. Recent developments in the synthesis of pyrazole derivatives. Heterocycles, 1985, 23(12), 3121-3153.
    • (1985) Heterocycles , vol.23 , Issue.12 , pp. 3121-3153
    • Elnagdi, M.H.1    Elgemeie, G.E.H.2    Abd-Elaal F.A.-E3
  • 13
    • 33645784098 scopus 로고    scopus 로고
    • Stereoselective cycloadditions of nitrilimines as a source of enantiopure heterocycles
    • Molteni, G. stereoselective cycloadditions of nitrilimines as a source of enantiopure heterocycles. Heterocycles, 2005, 65(10), 2513-2537.
    • (2005) Heterocycles , vol.65 , Issue.10 , pp. 2513-2537
    • Molteni, G.1
  • 14
    • 0842289719 scopus 로고    scopus 로고
    • Scorpionates: Genesis, milestones, prognosis
    • Trofimenko, S. Scorpionates: genesis, milestones, prognosis. Polyhedron, 2004, 23(2-3), 197-203.
    • (2004) Polyhedron , vol.23 , Issue.2-3 , pp. 197-203
    • Trofimenko, S.1
  • 15
    • 0034799031 scopus 로고    scopus 로고
    • Coordination and supramolecular chemistry of multinucleating ligands containing two or more pyrazolylpyridine 'arms'
    • Ward, M.D.; McCleverty, J.A.; Jeffery, J.C. Coordination and supramolecular chemistry of multinucleating ligands containing two or more pyrazolylpyridine 'arms'. Coord. Chem. Rev., 2001, 222(1), 251-272.
    • (2001) Coord. Chem. Rev , vol.222 , Issue.1 , pp. 251-272
    • Ward, M.D.1    McCleverty, J.A.2    Jeffery, J.C.3
  • 16
    • 0033803029 scopus 로고    scopus 로고
    • Coordination chemistry with pyrazole-based chelating ligands: Molecular structural aspects
    • Mukherjee, R. Coordination chemistry with pyrazole-based chelating ligands: molecular structural aspects. Coord. Chem. Rev., 2000, 203(1), 151-218.
    • (2000) Coord. Chem. Rev , vol.203 , Issue.1 , pp. 151-218
    • Mukherjee, R.1
  • 17
    • 0034749037 scopus 로고    scopus 로고
    • Progress in pyrazole chemistry
    • Sadimenko, A.P. Progress in pyrazole chemistry. Adv. Heterocycl. Chem., 2001, 80, 157-240.
    • (2001) Adv. Heterocycl. Chem , vol.80 , pp. 157-240
    • Sadimenko, A.P.1
  • 18
    • 0036096076 scopus 로고    scopus 로고
    • Synthesis and properties of acetylenic derivatives of pyrazoles
    • Vasilevsky, S.F.; Tretyakov, E.V.; Elguero, J. Synthesis and properties of acetylenic derivatives of pyrazoles. Adv. Heterocycl. Chem., 2002, 82, 1-99.
    • (2002) Adv. Heterocycl. Chem , vol.82 , pp. 1-99
    • Vasilevsky, S.F.1    Tretyakov, E.V.2    Elguero, J.3
  • 20
    • 0036736760 scopus 로고    scopus 로고
    • Unsaturated O- and N-heterocycles from carbohydrate feedstocks
    • Lichtenthaler, F.W. Unsaturated O- and N-heterocycles from carbohydrate feedstocks. Acc. Chem. Res., 2002, 35, 728-737.
    • (2002) Acc. Chem. Res , vol.35 , pp. 728-737
    • Lichtenthaler, F.W.1
  • 21
    • 0346394029 scopus 로고    scopus 로고
    • Structural revision in pyrazole chemistry
    • Kumar, D.; Singh, S.P. Structural revision in pyrazole chemistry. Heterocycles, 2004, 63(1), 145-173.
    • (2004) Heterocycles , vol.63 , Issue.1 , pp. 145-173
    • Kumar, D.1    Singh, S.P.2
  • 23
    • 11144220008 scopus 로고    scopus 로고
    • Pyrazol-3-ones. Part II: Reactions of the ring atoms
    • Varvounis, G.; Fiamegos, Y.; Pilidis, G. Pyrazol-3-ones. Part II: Reactions of the Ring Atoms. Adv. Heterocycl. Chem., 2004, 87, 141-272.
    • (2004) Adv. Heterocycl. Chem , vol.87 , pp. 141-272
    • Varvounis, G.1    Fiamegos, Y.2    Pilidis, G.3
  • 24
    • 37549069310 scopus 로고    scopus 로고
    • Pyrazol-3-ones. Part III: Reactivity of the ring substituents
    • Varvounis, G.; Fiamegos, Y.; Pilidis, G. Pyrazol-3-ones. Part III: Reactivity of the Ring Substituents. Adv. Heterocycl. Chem., 2007, 95, 27-141.
    • (2007) Adv. Heterocycl. Chem , vol.95 , pp. 27-141
    • Varvounis, G.1    Fiamegos, Y.2    Pilidis, G.3
  • 25
    • 33746556850 scopus 로고    scopus 로고
    • The calculated enthalpies of the nine pyrazole anions, cations, and radicals: A comparison with experiment
    • Alkorta, I.; Elguero, J. The calculated enthalpies of the nine pyrazole anions, cations, and radicals: a comparison with experiment. Tetrahedron, 2006, 62, 8683-8686.
    • (2006) Tetrahedron , vol.62 , pp. 8683-8686
    • Alkorta, I.1    Elguero, J.2
  • 27
    • 0345415478 scopus 로고    scopus 로고
    • Lithium-pyrazole-3,4,5-tricarbonitrile: Ion Pairing and Lithium Ion Affinity Studies
    • Markusson, H.; Béranger, S.; Johansson, P.; Armand, M.; Jacobsson, P. Lithium-pyrazole-3,4,5-tricarbonitrile: Ion Pairing and Lithium Ion Affinity Studies. J. Phys. Chem. A, 2003, 107, 10177-10183.
    • (2003) J. Phys. Chem. A , vol.107 , pp. 10177-10183
    • Markusson, H.1    Béranger, S.2    Johansson, P.3    Armand, M.4    Jacobsson, P.5
  • 29
    • 48549100882 scopus 로고    scopus 로고
    • 13C and 15N NMR chemical shifts of 1-(2',4'-dinitrophenyl) and 1-(2',4',6;-trinitrophenyl) pyrazoles in the solid state and in solution
    • García, M.A.; Claramunt, R.M.; Elguero, J. 13C and 15N NMR chemical shifts of 1-(2',4'-dinitrophenyl) and 1-(2',4',6;-trinitrophenyl) pyrazoles in the solid state and in solution. Magn. Reson. Chem., 2008, 46, 697-700.
    • (2008) Magn. Reson. Chem , vol.46 , pp. 697-700
    • García, M.A.1    Claramunt, R.M.2    Elguero, J.3
  • 30
    • 33646345854 scopus 로고    scopus 로고
    • 1H, 13C and 15N NMR study in solution and in the solid state of six N-substituted pyrazoles and indazoles
    • Claramunt, R.M.; Santa María, M.D.; Sanz, D.; Alkorta, I.; Elguero, J. A 1H, 13C and 15N NMR study in solution and in the solid state of six N-substituted pyrazoles and indazoles. Magn. Reson. Chem., 2006, 44(5), 566-570.
    • (2006) Magn. Reson. Chem , vol.44 , Issue.5 , pp. 566-570
    • Claramunt, R.M.1    Santa, M.M.D.2    Sanz, D.3    Alkorta, I.4    Elguero, J.A.5
  • 32
    • 75149166575 scopus 로고    scopus 로고
    • A theoretical comparison of the chemical shifts of three related heterocycles: 1 H-pyrazoles, 1H-1,2,4-triazoles and 1H-1,2,4-diazaphospholes
    • Alkorta, I.; Blanco, F.; Elguero, J. A theoretical comparison of the chemical shifts of three related heterocycles: 1 H-pyrazoles, 1H-1,2,4-triazoles and 1H-1,2,4-diazaphospholes. J. Mol. Struct. THEOCHEM, 2010, 942(1-3), 1-6.
    • (2010) J. Mol. Struct. THEOCHEM , vol.942 , Issue.1-3 , pp. 1-6
    • Alkorta, I.1    Blanco, F.2    Elguero, J.3
  • 33
    • 0035821428 scopus 로고    scopus 로고
    • A complete model for the prediction of 1H- and 13C-NMR chemical shifts and torsional angles in phenylsubstituted pyrazoles
    • Carrillo, J.R.; Cossío, F.P.; Díaz-Ortíz, A.; Gómez-Escalonilla, M.J.; de la Hoz, A.; Lecea, B.; Moreno, A.; Prieto, P. A complete model for the prediction of 1H- and 13C-NMR chemical shifts and torsional angles in phenylsubstituted pyrazoles. Tetrahedron, 2001, 57(19), 4179-4187.
    • (2001) Tetrahedron , vol.57 , Issue.19 , pp. 4179-4187
    • Carrillo, J.R.1    Cossío, F.P.2    Díaz-Ortíz, A.3    Gómez-Escalonilla, M.J.4    de la, H.A.5    Lecea, B.6    Moreno, A.7    Prieto, P.8
  • 34
    • 33846428817 scopus 로고    scopus 로고
    • Characterization of peptide-pyrazole interactions in solution by low-temperature NMR studies
    • Wang, W.; Weisz, K. characterization of peptide-pyrazole interactions in solution by low-temperature NMR studies. Chem. Eur. J., 2007, 13, 854-861.
    • (2007) Chem. Eur. J , vol.13 , pp. 854-861
    • Wang, W.1    Weisz, K.2
  • 35
    • 0036396046 scopus 로고    scopus 로고
    • Polymorphism vs. desmotropy: The cases of 3-Phenyl- and 5-Phenyl- 1Hpyrazoles and 3-Phenyl-1H-indazole
    • García, M.A.; López, C.; Claramunt, R.M.; Kenz, A.; Pierrot, M., Elguero, J. Polymorphism vs. desmotropy: The cases of 3-Phenyl- and 5-Phenyl- 1Hpyrazoles and 3-Phenyl-1H-indazole. Helv. Chim. Acta, 2002, 85(9), 2763-2776.
    • (2002) Helv. Chim. Acta , vol.85 , Issue.9 , pp. 2763-2776
    • García, M.A.1    López, C.2    Claramunt, R.M.3    Kenz, A.4    Pierrot, M.5    Elguero, J.6
  • 39
    • 0032793816 scopus 로고    scopus 로고
    • Aminopyrazoles and their conjugated acids. An X-ray study of 3,5-dimethyl- 4-aminopyrazole and the picrate of 3(5)-aminopyrazole
    • Infantes, L.; Foces-Foces, C.; Claramunt, R.-M.; Lopes, C.; Elguero, J. Aminopyrazoles and their conjugated acids. An X-ray study of 3,5-dimethyl- 4-aminopyrazole and the picrate of 3(5)-aminopyrazole. J. Heterocyl. Chem., 1999, 36(3), 595-600.
    • (1999) J. Heterocyl. Chem , vol.36 , Issue.3 , pp. 595-600
    • Infantes, L.1    Foces-Foces, C.2    Claramunt, R.-M.3    Lopes, C.4    Elguero, J.5
  • 40
    • 0037454715 scopus 로고    scopus 로고
    • The structure of the agrochemical fungicidal 4-chloro-3-(3,5-dichlorophenyl)-1H-pyrazole (RPA 406194) and related compounds
    • Vors, J.-P.; Gerbaud, V.; Gabas, N.; Canselier, J.P.; Jagerovic, N.; Jimenoc, M.L.; Elguero, J. The structure of the agrochemical fungicidal 4-chloro-3-(3,5-dichlorophenyl)-1H-pyrazole (RPA 406194) and related compounds. Tetrahedron, 2003, 59(4), 555-560.
    • (2003) Tetrahedron , vol.59 , Issue.4 , pp. 555-560
    • Vors, J.-P.1    Gerbaud, V.2    Gabas, N.3    Canselier, J.P.4    Jagerovic, N.5    Jimenoc, M.L.6    Elguero, J.7
  • 41
    • 40649101845 scopus 로고    scopus 로고
    • A molecular balance to measure the strength of N-H π hydrogen bonds based on the tautomeric equilibria of C-benzylphenyl substituted NH-pyrazoles
    • Cornago, P.; Claramunt, R.M.; Bouissane, L.; Elguero, J. A molecular balance to measure the strength of N-H π hydrogen bonds based on the tautomeric equilibria of C-benzylphenyl substituted NH-pyrazoles. Tetrahedron, 2008, 64, 3667-3673.
    • (2008) Tetrahedron , vol.64 , pp. 3667-3673
    • Cornago, P.1    Claramunt, R.M.2    Bouissane, L.3    Elguero, J.4
  • 43
    • 19544363799 scopus 로고    scopus 로고
    • Obrazovanie nesimmetrichnyh 2- (diacilmetilen)-2,3-digidro-1H-benzimidazolov pri acidolize 1-benzoil-2-(bbenzoiloksi- b-fenilvinil)-1H-benzimidazola
    • Dzvinchuk, I.B.; Lozinskii, M.O. Obrazovanie nesimmetrichnyh 2- (diacilmetilen)-2,3-digidro-1H-benzimidazolov pri acidolize 1-benzoil-2-(bbenzoiloksi- b-fenilvinil)-1H-benzimidazola. Khim. Geterotsikl. Soedin., 2001, 606-612;
    • (2001) Khim. Geterotsikl. Soedin , pp. 606-612
    • Dzvinchuk, I.B.1    Lozinskii, M.O.2
  • 44
    • 0345977281 scopus 로고    scopus 로고
    • Formation of Unsymmetrical 2-(Diacylmethylene)-2,3- dihydro-1H-benzimidazoles During Acidolysis of 1-Benzoyl-2-(β- benzoyloxy- β-phenylvinyl)-1H-benzimidazole
    • Formation of Unsymmetrical 2-(Diacylmethylene)-2,3- dihydro-1H-benzimidazoles During Acidolysis of 1-Benzoyl-2-(β- benzoyloxy- β-phenylvinyl)-1H-benzimidazole. Chem. Heterocyclic Comp., 2001, 37(5), 554-559.
    • (2001) Chem. Heterocyclic Comp , vol.37 , Issue.5 , pp. 554-559
  • 45
    • 55149117850 scopus 로고    scopus 로고
    • Sintez i tautomeriya 2-[3(5)- aril(metil)pirazol-4-il]-1-benzimidazolov
    • Dzvinchuk, I.B.; Lozinskii, M.O. Sintez i tautomeriya 2-[3(5)-aril(metil)pirazol-4-il]-1-benzimidazolov. Khim. Geterotsikl. Soedin., 2006, 1370-1378;
    • (2006) Khim. Geterotsikl. Soedin , pp. 1370-1378
    • Dzvinchuk, I.B.1    Lozinskii, M.O.2
  • 46
    • 33845510685 scopus 로고    scopus 로고
    • Synthesis and tautomerism of 2-[3(5)-aryl(methyl)pyrazol-4-yl]- 1-benzimidazoles
    • Synthesis and tautomerism of 2-[3(5)-aryl(methyl)pyrazol-4-yl]- 1-benzimidazoles. Chem. Heterocycl. Comp., 2006, 42(9), 1190-1196.
    • (2006) Chem. Heterocycl. Comp , vol.42 , Issue.9 , pp. 1190-1196
  • 48
    • 33845379599 scopus 로고
    • Dynamic intermolecular tautomerism of 3,5-dimethylpyrazole in the solid state by carbon- 13 CP/MAS NMR spectroscopy and x-ray crystallography
    • Baldy, A.; Elguero, J.; Faure, R.; Pierrot, M.; Vincent, E.-J. Dynamic intermolecular tautomerism of 3,5-dimethylpyrazole in the solid state by carbon- 13 CP/MAS NMR spectroscopy and x-ray crystallography. J. Am. Chem. Soc., 1985, 107(18), 5290-5291.
    • (1985) J. Am. Chem. Soc , vol.107 , Issue.18 , pp. 5290-5291
    • Baldy, A.1    Elguero, J.2    Faure, R.3    Pierrot, M.4    Vincent, E.-J.5
  • 49
    • 0034815821 scopus 로고    scopus 로고
    • A solid-state NMR, x-ray diffraction, and ab initio computational study of hydrogen-bond structure and dynamics of pyrazole-4-carboxylic acid chains
    • Foces-Foces, C.; Echevarría, A.; Jagerovic, N.; Alkorta, I.; Elguero, J.; Langer, U.; Klein, O.; Minguet-Bonvehí, M.; Limbach, H.-H. a solid-state NMR, x-ray diffraction, and ab initio computational study of hydrogen-bond structure and dynamics of pyrazole-4-carboxylic acid chains. J. Am. Chem. Soc., 2001, 123(32), 7898-7906.
    • (2001) J. Am. Chem. Soc , vol.123 , Issue.32 , pp. 7898-7906
    • Foces-Foces, C.1    Echevarría, A.2    Jagerovic, N.3    Alkorta, I.4    Elguero, J.5    Langer, U.6    Klein, O.7    Minguet-Bonvehí, M.8    Limbach, H.-H.9
  • 50
    • 1442275753 scopus 로고    scopus 로고
    • Kinetic hydrogen/ deuterium isotope effects in multiple proton transfer reactions
    • Limbach, H.-H.; Klein, O.; López del Amo, J.M.; Elguero, J. Kinetic hydrogen/ deuterium isotope effects in multiple proton transfer reactions. Z. Phys. Chem., 2004, 218(1), 17-49.
    • (2004) Z. Phys. Chem , vol.218 , Issue.1 , pp. 17-49
    • Limbach, H.-H.1    Klein, O.2    López del Amo, J.M.3    Elguero, J.4
  • 51
    • 33644644738 scopus 로고    scopus 로고
    • Pyrazoles as molecular probes to study the properties of co-crystals by solid state NMR spectroscopy
    • López, C.; Claramunt, R.M.; García, M.A.; Elguero, J. Pyrazoles as molecular probes to study the properties of co-crystals by solid state NMR spectroscopy. Cent. Eur. J. Chem., 2004, 2(4), 660-671.
    • (2004) Cent. Eur. J. Chem , vol.2 , Issue.4 , pp. 660-671
    • López, C.1    Claramunt, R.M.2    García, M.A.3    Elguero, J.4
  • 52
    • 46249113822 scopus 로고    scopus 로고
    • Proton transfer in C -halogen pyrazole cyclamers. A theoretical study
    • Alkorta, I.; Blanco, F.; Elguero, J. Proton transfer in C -halogen pyrazole cyclamers. A theoretical study. Struct. Chem., 2008, 19, 191-198.
    • (2008) Struct. Chem , vol.19 , pp. 191-198
    • Alkorta, I.1    Blanco, F.2    Elguero, J.3
  • 53
    • 33644913976 scopus 로고    scopus 로고
    • Double proton transfer reactions with plateau-like transition state regions: Pyrazole-trifluoroacetic acid clusters
    • Schweiger, S.; Rauhut, G. double proton transfer reactions with plateau-like transition state regions: pyrazole-trifluoroacetic acid clusters. J. Phys. Chem. A, 2006, 110, 2816-2820.
    • (2006) J. Phys. Chem. A , vol.110 , pp. 2816-2820
    • Schweiger, S.1    Rauhut, G.2
  • 54
    • 0042233915 scopus 로고    scopus 로고
    • Excited-state intramolecular proton transfer in five-membered hydrogen-bonding systems: 2-pyridyl pyrazoles
    • Yu, W.S.; Cheng, C.-C.; Cheng, Y.-M.; Wu, P.-C.; Song, Y.H.; Chi, Y.; Chou, P.-T. excited-state intramolecular proton transfer in five-membered hydrogen-bonding systems: 2-pyridyl pyrazoles. J. Am. Chem. Soc., 2003, 125(36), 10800-10801.
    • (2003) J. Am. Chem. Soc , vol.125 , Issue.36 , pp. 10800-10801
    • Yu, W.S.1    Cheng, C.-C.2    Cheng, Y.-M.3    Wu, P.-C.4    Song, Y.H.5    Chi, Y.6    Chou, P.-T.7
  • 55
    • 39349106836 scopus 로고    scopus 로고
    • Retro-[3 + 2]-cycloaddition reactions in the decomposition of five-membered nitrogen-containing heterocycles
    • da Silva, G.; Bozzelli, J.W. retro-[3 + 2]-cycloaddition reactions in the decomposition of five-membered nitrogen-containing heterocycles. J. Org. Chem., 2008, 73, 1343-1353.
    • (2008) J. Org. Chem , vol.73 , pp. 1343-1353
    • da Silva, G.1    Bozzelli, J.W.2
  • 56
    • 17744362499 scopus 로고    scopus 로고
    • Role of conformation and electronic structure in the chemistry of ground and excited state o-pyrazolylphenylnitrenes
    • Carra, C.; Bally, T.; Albini, A. role of conformation and electronic structure in the chemistry of ground and excited state o-pyrazolylphenylnitrenes. J. Am. Chem. Soc., 2005, 127, 5552-5562.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 5552-5562
    • Carra, C.1    Bally, T.2    Albini, A.3
  • 57
    • 0035804939 scopus 로고    scopus 로고
    • Flash vacuum pyrolysis over solid catalysts. 1. pyrazoles over zeolites
    • Moyano, E.L.; Yranzo, G.I. flash vacuum pyrolysis over solid catalysts. 1. pyrazoles over zeolites. J. Org. Chem., 2001, 66, 2943-2947.
    • (2001) J. Org. Chem , vol.66 , pp. 2943-2947
    • Moyano, E.L.1    Yranzo, G.I.2
  • 58
    • 0037111682 scopus 로고    scopus 로고
    • Flash vacuum pyrolysis over solid catalysts. 2. pyrazoles over hydrotalcites
    • Moyano, E.L.; del Arco, M.; Rives, V.; Yranzo, G.I. Flash vacuum pyrolysis over solid catalysts. 2. pyrazoles over hydrotalcites. J. Org. Chem., 2002, 67, 8147-8150.
    • (2002) J. Org. Chem , vol.67 , pp. 8147-8150
    • Moyano, E.L.1    del Arco, M.2    Rives, V.3    Yranzo, G.I.4
  • 59
    • 0036712012 scopus 로고    scopus 로고
    • Switchable reactivity: The site-selective functionalization of trifluoromethyl-substituted pyrazoles
    • Schlosser, M.; Volle, J.-N.; Leroux, F.; Schenk, K. Switchable reactivity: the site-selective functionalization of trifluoromethyl-substituted pyrazoles. Eur. J. Org. Chem., 2002, (17), 2913-2920.
    • (2002) Eur. J. Org. Chem , vol.17 , pp. 2913-2920
    • Schlosser, M.1    Volle, J.-N.2    Leroux, F.3    Schenk, K.4
  • 60
    • 0037696879 scopus 로고    scopus 로고
    • New pyrazoliumcarboxylates as structural analogues of the pseudo-cross-conjugated betainic alkaloid nigellicine
    • Schmidt, A.; Habeck, T.; Kindermann, M.K.; Nieger, M. new pyrazoliumcarboxylates as structural analogues of the pseudo-cross-conjugated betainic alkaloid nigellicine. J. Org. Chem., 2003, 68(15), 5977-5982.
    • (2003) J. Org. Chem , vol.68 , Issue.15 , pp. 5977-5982
    • Schmidt, A.1    Habeck, T.2    Kindermann, M.K.3    Nieger, M.4
  • 61
    • 19844383213 scopus 로고    scopus 로고
    • Nucleophilic carbenes of pyrazoles starting from pseudo-cross-conjugated mesomeric betaines
    • Schmidt, A.; Habeck, T. nucleophilic carbenes of pyrazoles starting from pseudo-cross-conjugated mesomeric betaines. Lett. Org. Chem., 2005, 2(1), 37-39.
    • (2005) Lett. Org. Chem , vol.2 , Issue.1 , pp. 37-39
    • Schmidt, A.1    Habeck, T.2
  • 62
    • 79958226857 scopus 로고    scopus 로고
    • Funktionalisierte 4-aminochinoline durch umlagerung von n-heterocyclischen carbenen des pyrazols
    • Schmidt, A.; Münster, N.; Dreger, A. funktionalisierte 4-aminochinoline durch umlagerung von n-heterocyclischen carbenen des pyrazols. Angew. Chem., 2010, 122(15), 2851-2854;
    • (2010) Angew. Chem , vol.122 , Issue.15 , pp. 2851-2854
    • Schmidt, A.1    Münster, N.2    Dreger, A.3
  • 63
    • 77950504117 scopus 로고    scopus 로고
    • Functionalized 4-aminoquinolines by rearrangement of pyrazole N-heterocyclic carbenes
    • Functionalized 4-aminoquinolines by rearrangement of pyrazole N-heterocyclic carbenes. Angew. Chem. Int. Ed., 2010, 49(15), 2790-2793.
    • (2010) Angew. Chem. Int. Ed , vol.49 , Issue.15 , pp. 2790-2793
  • 64
    • 77954970942 scopus 로고    scopus 로고
    • Rearrangements of n-heterocyclic carbenes of pyrazole to 4- aminoquinolines and benzoquinolines
    • Dreger, A.; Cisneros Camuña, R.; Münster, N.; Rokob, T.A.; Pápai, I.; Schmidt, A. rearrangements of n-heterocyclic carbenes of pyrazole to 4- aminoquinolines and benzoquinolines. Eur. J. Org. Chem., 2010, (22), 4296-4305.
    • (2010) Eur. J. Org. Chem , vol.22 , pp. 4296-4305
    • Dreger, A.1    Cisneros, C.R.2    Münster, N.3    Rokob, T.A.4    Pápai, I.5    Schmidt, A.6
  • 65
    • 55149119722 scopus 로고    scopus 로고
    • A theoretical insight into the reaction mechanism of photochemical transposition from pyrazole to imidazole
    • Su, M.-D. A theoretical insight into the reaction mechanism of photochemical transposition from pyrazole to imidazole. J. Phys. Chem. A, 2008, 112(41), 10420-10428.
    • (2008) J. Phys. Chem. A , vol.112 , Issue.41 , pp. 10420-10428
    • Su, M.-D.1
  • 66
    • 23944509573 scopus 로고    scopus 로고
    • Synthesis of new 3h-pyrazoles and cyclopropenyl alcohols directly from propargyl alcohols
    • Hamdi, N.; Dixneuf, P.H.; Khemiss, A. synthesis of new 3h-pyrazoles and cyclopropenyl alcohols directly from propargyl alcohols. Eur. J. Org. Chem., 2005, (16), 3526-3529.
    • (2005) Eur. J. Org. Chem , vol.16 , pp. 3526-3529
    • Hamdi, N.1    Dixneuf, P.H.2    Khemiss, A.3
  • 67
    • 0009401381 scopus 로고
    • Withasomnine. A pyrazole alkaloid from Withania somnifera Dun
    • Schröter, H.B.; Neumann, D.; Katritzky, A.R.; Swinbourne, F.J. Withasomnine. A pyrazole alkaloid from Withania somnifera Dun. Tetrahedron, 1966, 22(8), 2895-2897.
    • (1966) Tetrahedron , vol.22 , Issue.8 , pp. 2895-2897
    • Schröter, H.B.1    Neumann, D.2    Katritzky, A.R.3    Swinbourne, F.J.4
  • 68
    • 0037013971 scopus 로고    scopus 로고
    • Radical cyclisation onto pyrazoles: Synthesis of withasomnine
    • Allin, S.M.; Barton, W.R.S.; Bowman, W.R.; McInally, T. Radical cyclisation onto pyrazoles: synthesis of withasomnine. Tetrahedron Lett., 2002, 43, 4191-4193.
    • (2002) Tetrahedron Lett , vol.43 , pp. 4191-4193
    • Allin, S.M.1    Barton, W.R.S.2    Bowman, W.R.3    McInally, T.4
  • 69
    • 0028001924 scopus 로고
    • Pyrazole alkaloids from Newbouldia laevis
    • Adesanya, S.A.; Nia, R.; Fontaine, C.; Païs, M. Pyrazole alkaloids from Newbouldia laevis. Phytochemistry, 1994, 35(4), 1053-1055.
    • (1994) Phytochemistry , vol.35 , Issue.4 , pp. 1053-1055
    • Adesanya, S.A.1    Nia, R.2    Fontaine, C.3    Païs, M.4
  • 70
    • 0031985265 scopus 로고    scopus 로고
    • New pyrazole alkaloids from the root bark of Newbouldia laevis
    • Aladesanmi, A.J.; Nia, R.; Nahrstedt, A. New pyrazole alkaloids from the root bark of Newbouldia laevis. Planta Med., 1998, 64, 90-91.
    • (1998) Planta Med , vol.64 , pp. 90-91
    • Aladesanmi, A.J.1    Nia, R.2    Nahrstedt, A.3
  • 71
    • 39149100002 scopus 로고    scopus 로고
    • Constituents of the stem bark of Discopodium penninervium and their LTB4 and COX-1 and -2 inhibitory activities
    • Wube, A.A.; Wenzig, E.-M.; Gibbons, S.; Asres, K.; Bauer, R.; Bucar, F. Constituents of the stem bark of Discopodium penninervium and their LTB4 and COX-1 and -2 inhibitory activities. Phytochemistry, 2008, 69, 982-987.
    • (2008) Phytochemistry , vol.69 , pp. 982-987
    • Wube, A.A.1    Wenzig, E.-M.2    Gibbons, S.3    Asres, K.4    Bauer, R.5    Bucar, F.6
  • 73
    • 0542371982 scopus 로고    scopus 로고
    • Heteroaromatic acid from marine sponge Suberites vestigium
    • Mishra, P.D.; Wahidullah, S.; Kamat, S.Y. A heteroaromatic acid from marine sponge Suberites vestigium. Indian J. Chem., Sect. B, 1998, 37B(2), 199-200.
    • (1998) Indian J. Chem., Sect. B , vol.37 B , Issue.2 , pp. 199-200
    • Mishra, P.D.1    Wahidullah, S.2    Kamat, S.Y.A.3
  • 74
    • 0030796455 scopus 로고    scopus 로고
    • Secondary metabolites from the sponge tedania anhelans: Isolation and characterization of two novel pyrazole acids and other metabolites
    • Parameswaran, P.S.; Naik, C.G.; Hegde, V.R. secondary metabolites from the sponge tedania anhelans: isolation and characterization of two novel pyrazole acids and other metabolites. J. Nat. Prod., 1997, 60(8), 802-803.
    • (1997) J. Nat. Prod , vol.60 , Issue.8 , pp. 802-803
    • Parameswaran, P.S.1    Naik, C.G.2    Hegde, V.R.3
  • 75
    • 0038203630 scopus 로고    scopus 로고
    • New manzamine alkaloids with activity against infectious and tropical parasitic diseases from an indonesian sponge
    • Rao, K.V.; Santarsiero, B.D.; Mesecar, A.D.; Schinazi, R.F.; Tekwani, B.L. Hamann, M.T.; new manzamine alkaloids with activity against infectious and tropical parasitic diseases from an indonesian sponge. J. Nat. Prod., 2003, 66, 823-828.
    • (2003) J. Nat. Prod , vol.66 , pp. 823-828
    • Rao, K.V.1    Santarsiero, B.D.2    Mesecar, A.D.3    Schinazi, R.F.4    Tekwani, B.L.5    Hamann, M.T.6
  • 76
    • 0001221337 scopus 로고
    • The synthesis of L-α-amino- β- (pyrazolyl-N)-propionic acid in Citrullus vulgaris
    • Sugimoto, N.; Watanabe, H.; Ide, A. The synthesis of L-α-amino- β- (pyrazolyl-N)-propionic acid in Citrullus vulgaris. Tetrahedron, 1960, 11(4), 231-233.
    • (1960) Tetrahedron , vol.11 , Issue.4 , pp. 231-233
    • Sugimoto, N.1    Watanabe, H.2    Ide, A.3
  • 77
    • 51149219272 scopus 로고
    • C-Nucleoside studies. Part 14. A new synthesis of pyrazofurin
    • Buchanan, J.G.; Stobie, A.; Wightman, R.H. C-Nucleoside studies. Part 14. A new synthesis of pyrazofurin. J. Chem. Soc., Perkin Trans. 1, 1981, (8), 2374-2378.
    • (1981) J. Chem. Soc. Perkin Trans , vol.1 , Issue.8 , pp. 2374-2378
    • Buchanan, J.G.1    Stobie, A.2    Wightman, R.H.3
  • 78
    • 33750865454 scopus 로고    scopus 로고
    • The chemistry of c-nucleosides and their analogs i: C-nucleosides of hetero monocyclic bases
    • Shaban, M.A.E.; Nasr, A.Z. the chemistry of c-nucleosides and their analogs i: c-nucleosides of hetero monocyclic bases. Adv. Heterocycl. Chem., 1997, 68, 223-432.
    • (1997) Adv. Heterocycl. Chem , vol.68 , pp. 223-432
    • Shaban, M.A.E.1    Nasr, A.Z.2
  • 80
    • 36549013145 scopus 로고    scopus 로고
    • Pyrazole chemistry in crop protection
    • Lamberth, C. Pyrazole chemistry in crop protection. Heterocycles, 2007, 71(7), 1467-1502.
    • (2007) Heterocycles , vol.71 , Issue.7 , pp. 1467-1502
    • Lamberth, C.1
  • 81
    • 42249084709 scopus 로고    scopus 로고
    • Antifungal and antimycobacterial activity of 1-(3,5-diaryl-4,5-dihydro-1Hpyrazol-4-yl)-1H-imidazole derivatives
    • Zampieri, D.; Mamolo, M.G.; Laurini, E.; Scialino, G.; Banfi, E.; Vio, L. Antifungal and antimycobacterial activity of 1-(3,5-diaryl-4,5-dihydro-1Hpyrazol-4-yl)-1H-imidazole derivatives. Bioorg. Med. Chem., 2008, 16, 4516-4522.
    • (2008) Bioorg. Med. Chem , vol.16 , pp. 4516-4522
    • Zampieri, D.1    Mamolo, M.G.2    Laurini, E.3    Scialino, G.4    Banfi, E.5    Vio, L.6
  • 82
    • 0028172369 scopus 로고
    • Inhibition by SK&F 96365 of Ca2+ current, IL-2 production and activation in T lymphocytes
    • Chung, S.C.; McDonald, T.V.; Gardner, P. Inhibition by SK&F 96365 of Ca2+ current, IL-2 production and activation in T lymphocytes. Br. J. Pharmacol., 1994, 113(3), 861-868.
    • (1994) Br. J. Pharmacol , vol.113 , Issue.3 , pp. 861-868
    • Chung, S.C.1    McDonald, T.V.2    Gardner, P.3
  • 84
    • 33645665682 scopus 로고    scopus 로고
    • Discovery of 4-{4-[3-(Pyridin-2-yl)-1H-pyrazol-4-yl] pyridin-2-yl}-N-(tetrahydro-2H- pyran-4-yl) benzamide (GW788388): A potent, selective, and orally active transforming growth factor- β Type I receptor inhibitor
    • Gellibert, F.; de Gouville, A.-C.; Woolven, J.; Mathews, N.; Nguyen, V.-L.; Bertho-Ruault, C.; Patikis, A.; Grygielko, E.T.; Laping, N.J.; Huet, S. Discovery of 4-{4-[3-(Pyridin-2-yl)-1H-pyrazol-4-yl] pyridin-2-yl}-N-(tetrahydro-2H- pyran-4-yl) benzamide (GW788388): A potent, selective, and orally active transforming growth factor- β Type I receptor inhibitor. J. Med. Chem., 2006, 49, 2210-2221.
    • (2006) J. Med. Chem , vol.49 , pp. 2210-2221
    • Gellibert, F.1    de Gouville, A.-C.2    Woolven, J.3    Mathews, N.4    Nguyen, V.-L.5    Bertho-Ruault, C.6    Patikis, A.7    Grygielko, E.T.8    Laping, N.J.9    Huet, S.10
  • 85
    • 38949111028 scopus 로고    scopus 로고
    • Selective, high affinity A2B adenosine receptor antagonists: N-1 monosubstituted 8-(pyrazol-4-yl)xanthines
    • Kalla, R.V.; Elzein, E.; Perry, T.; Li, X.; Gimbel, A.; Yang, M.; Zeng, D.; Zablocki, J. Selective, high affinity A2B adenosine receptor antagonists: N-1 monosubstituted 8-(pyrazol-4-yl)xanthines. Bioorg. Med. Chem. Lett., 2008, 18, 1397-1401.
    • (2008) Bioorg. Med. Chem. Lett , vol.18 , pp. 1397-1401
    • Kalla, R.V.1    Elzein, E.2    Perry, T.3    Li, X.4    Gimbel, A.5    Yang, M.6    Zeng, D.7    Zablocki, J.8
  • 86
    • 41849134287 scopus 로고    scopus 로고
    • 5-tert-Butyl-N-pyrazol-4-yl-4,5,6,7-tetrahydrobenzo[d]isoxazole- 3-carboxamide derivatives as novel potent inhibitors of Mycobacterium tuberculosis pantothenate synthetase: Initiating a quest for New antitubercular drugs
    • Velaparthi, S.; Brunsteiner, M.; Uddin, R.; Wan, B.; Franzblau, S.G.; Petukhov, P.A. 5-tert-Butyl-N-pyrazol-4-yl-4,5,6,7-tetrahydrobenzo[d]isoxazole- 3-carboxamide derivatives as novel potent inhibitors of Mycobacterium tuberculosis pantothenate synthetase: Initiating a quest for New antitubercular drugs. J. Med. Chem., 2008, 51, 1999-2002.
    • (2008) J. Med. Chem , vol.51 , pp. 1999-2002
    • Velaparthi, S.1    Brunsteiner, M.2    Uddin, R.3    Wan, B.4    Franzblau, S.G.5    Petukhov, P.A.6
  • 87
    • 36148964016 scopus 로고    scopus 로고
    • Synthesis and evaluation of antiparasitic activities of new 4-[5-(4- Phenoxyphenyl)-2H-pyrazol-3-yl] morpholine derivatives
    • Kuettel, S.; Zambon, A.; Kaiser, M.; Brun, R.; Scapozza, L.; Perozzo, R. synthesis and evaluation of antiparasitic activities of new 4-[5-(4- Phenoxyphenyl)-2H-pyrazol-3-yl] morpholine derivatives. J. Med. Chem., 2007, 50, 5833-5839.
    • (2007) J. Med. Chem , vol.50 , pp. 5833-5839
    • Kuettel, S.1    Zambon, A.2    Kaiser, M.3    Brun, R.4    Scapozza, L.5    Perozzo, R.6
  • 91
    • 33750522014 scopus 로고    scopus 로고
    • Identification of 2-hydroxymethyl-4-[5-(4-methoxyphenyl)-3-trifluoromethyl-pyrazol-1-yl]-N-propionylbenzenesulfonamide sodium as a potential COX-2 inhibitor for oral and parenteral administration
    • Singh, S.K.; Vobbalareddy, S.; Kalleda, S.R.; Casturi, S.R.; Datla, S.R.; Mamidi, R.N.V.S.; Mullangi, R.; Ramanujam, R.; Yeleswarapu, K.R.; Iqbal, J. Identification of 2-hydroxymethyl-4-[5-(4-methoxyphenyl)-3-trifluoromethyl-pyrazol-1-yl]-N-propionylbenzenesulfonamide sodium as a potential COX-2 inhibitor for oral and parenteral administration. Bioorg. Med. Chem., 2006, 14, 8626-8634.
    • (2006) Bioorg. Med. Chem , vol.14 , pp. 8626-8634
    • Singh, S.K.1    Vobbalareddy, S.2    Kalleda, S.R.3    Casturi, S.R.4    Datla, S.R.5    Mamidi, R.N.V.S.6    Mullangi, R.7    Ramanujam, R.8    Yeleswarapu, K.R.9    Iqbal, J.10
  • 92
    • 33847783301 scopus 로고    scopus 로고
    • Synthesis and in vivo evaluation of [18F]-4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1Hpyrazol- 1-yl] benzenesulfonamide as a PET imaging probe for COX-2 expression
    • Prabhakaran, J.; Underwood, M.D.; Parsey, V.R.; Arango, V.; Majo, V.J.; Simpson, N.R.; Van Heertum, R.; Mann, J.J.; Kumar, J.S.D. Synthesis and in vivo evaluation of [18F]-4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1Hpyrazol- 1-yl] benzenesulfonamide as a PET imaging probe for COX-2 expression. Bioorg. Med. Chem., 2007, 15, 1802-1807.
    • (2007) Bioorg. Med. Chem , vol.15 , pp. 1802-1807
    • Prabhakaran, J.1    Underwood, M.D.2    Parsey, V.R.3    Arango, V.4    Majo, V.J.5    Simpson, N.R.6    van Heertum, R.7    Mann, J.J.8    Kumar, J.S.D.9
  • 95
    • 33646821317 scopus 로고    scopus 로고
    • Novel potent and selective calcium-release-activated calcium (CRAC) channel inhibitors. Part 1: Synthesis and inhibitory activity of 5-(1-methyl-3-trifluoromethyl-1Hpyrazol-5-yl)-2-thiophenecarboxamides
    • Yonetoku, Y.; Kubota, H.; Okamoto, Y.; Toyoshima, A.; Funatsu, M.; Ishikawa, J.; Takeuchi, M.; Ohta, M.; Tsukamoto, S.-I. Novel potent and selective calcium-release-activated calcium (CRAC) channel inhibitors. Part 1: Synthesis and inhibitory activity of 5-(1-methyl-3-trifluoromethyl-1Hpyrazol-5-yl)-2-thiophenecarboxamides. Bioorg. Med. Chem., 2006, 14, 4750-4760.
    • (2006) Bioorg. Med. Chem , vol.14 , pp. 4750-4760
    • Yonetoku, Y.1    Kubota, H.2    Okamoto, Y.3    Toyoshima, A.4    Funatsu, M.5    Ishikawa, J.6    Takeuchi, M.7    Ohta, M.8    Tsukamoto, S.-I.9
  • 98
    • 47349110358 scopus 로고    scopus 로고
    • Synthesis and discovery of autophagy inducers for A549 and H460 lung cancer cells, novel 1-(2'-hydroxy-3'-aroxypropyl)-3-aryl-1H-pyrazole-5- carbohydrazide derivatives
    • Fan, C.-D.; Zhao, B.-X.; Wie, F.; Zhang, G.-H.; Dong, W.-L.; Miao, J.-Y. Synthesis and discovery of autophagy inducers for A549 and H460 lung cancer cells, novel 1-(2'-hydroxy-3'-aroxypropyl)-3-aryl-1H-pyrazole-5- carbohydrazide derivatives. Bioorg. Med. Chem. Lett., 2008, 18, 3860-3864.
    • (2008) Bioorg. Med. Chem. Lett , vol.18 , pp. 3860-3864
    • Fan, C.-D.1    Zhao, B.-X.2    Wie, F.3    Zhang, G.-H.4    Dong, W.-L.5    Miao, J.-Y.6
  • 101
    • 48149103866 scopus 로고    scopus 로고
    • Convenient access to 1,3,4-trisubstituted pyrazoles carrying 5-nitrothiophene moiety via 1,3-dipolar cycloaddition of sydnones with acetylenic ketones and their antimicrobial evaluation
    • Rai, N.S.; Kalluraya, B.; Lingappa, B.; Shenoy, S.; Puranic, V.G. Convenient access to 1,3,4-trisubstituted pyrazoles carrying 5-nitrothiophene moiety via 1,3-dipolar cycloaddition of sydnones with acetylenic ketones and their antimicrobial evaluation. Eur. J. Med. Chem., 2008, 43, 1715-1720.
    • (2008) Eur. J. Med. Chem , vol.43 , pp. 1715-1720
    • Rai, N.S.1    Kalluraya, B.2    Lingappa, B.3    Shenoy, S.4    Puranic, V.G.5
  • 102
    • 33745143300 scopus 로고    scopus 로고
    • N-Acylated sulfonamide sodium salt: A prodrug of choice for the bifunctional 2-hydroxymethyl-4-(5- phenyl-3-trifluoromethyl-pyrazol-1-yl) benzenesulfonamide class of COX-2 inhibitors
    • Singh, S.K.; Vobbalareddy, S.; Kalleda, S.R.; Casturi, S.R.; Mullangi, R.; Ramanujam, R.; Yeleswarapu, K.R.; Iqbal, J. N-Acylated sulfonamide sodium salt: A prodrug of choice for the bifunctional 2-hydroxymethyl-4-(5- phenyl-3-trifluoromethyl-pyrazol-1-yl) benzenesulfonamide class of COX-2 inhibitors. Bioorg. Med. Chem. Lett., 2006, 16, 3921-3926.
    • (2006) Bioorg. Med. Chem. Lett , vol.16 , pp. 3921-3926
    • Singh, S.K.1    Vobbalareddy, S.2    Kalleda, S.R.3    Casturi, S.R.4    Mullangi, R.5    Ramanujam, R.6    Yeleswarapu, K.R.7    Iqbal, J.8
  • 103
    • 8644252687 scopus 로고    scopus 로고
    • Discovery of positive allosteric modulators for the metabotropic glutamate Receptor Subtype 5 from a Series of N-(1,3-Diphenyl-1H- pyrazol-5-yl)benzamides that potentiate receptor function in vivo
    • Lindsley, C.W.; Wisnoski, D.D.; Duggan, M.E.; Leister, W.H.; Hartman, G.D.; Huff, J.R.; Williams, D.L.; ÓBrien, J.A.; Lemaire, W.; Sur, C. Discovery of positive allosteric modulators for the metabotropic glutamate Receptor Subtype 5 from a Series of N-(1,3-Diphenyl-1H- pyrazol-5-yl)benzamides that potentiate receptor function in vivo. J. Med. Chem., 2004, 47(24), 5825-5828.
    • (2004) J. Med. Chem , vol.47 , Issue.24 , pp. 5825-5828
    • Lindsley, C.W.1    Wisnoski, D.D.2    Duggan, M.E.3    Leister, W.H.4    Hartman, G.D.5    Huff, J.R.6    Williams, D.L.7    ÓBrien, J.A.8    Lemaire, W.9    Sur, C.10
  • 105
    • 33744801125 scopus 로고    scopus 로고
    • Substituent effects of N-(1,3- diphenyl-1H-pyrazol-5-yl)benzamides on positive allosteric modulation of the metabotropic glutamate-5 receptor in rat cortical astrocytes
    • de Paulis, T.; Hemstapat, K.; Chen, Y.; Zhang, Y.; Saleh, S.; Alagille, D.; Baldwin, R.M.; Tamagnan, G.D.; Conn, P.J. Substituent effects of N-(1,3- diphenyl-1H-pyrazol-5-yl)benzamides on positive allosteric modulation of the metabotropic glutamate-5 receptor in rat cortical astrocytes. J. Med. Chem., 2006, 49, 3332-3344.
    • (2006) J. Med. Chem , vol.49 , pp. 3332-3344
    • de Paulis, T.1    Hemstapat, K.2    Chen, Y.3    Zhang, Y.4    Saleh, S.5    Alagille, D.6    Baldwin, R.M.7    Tamagnan, G.D.8    Conn, P.J.9
  • 110
    • 48449100032 scopus 로고    scopus 로고
    • Synthesis and antiviral evaluation of some new pyrazole and fused pyrazolopyrimidine derivatives
    • Rashad, A.E.; Hegab, M.I.; Abdel-Megeid, R.E.; Micky, J.A.; Abdel- Megeid, F.M.E. Synthesis and antiviral evaluation of some new pyrazole and fused pyrazolopyrimidine derivatives. Bioorg. Med. Chem., 2008, 16, 7102-7106.
    • (2008) Bioorg. Med. Chem , vol.16 , pp. 7102-7106
    • Rashad, A.E.1    Hegab, M.I.2    Abdel-Megeid, R.E.3    Micky, J.A.4    Abdel-Megeid, F.M.E.5
  • 112
    • 44849132107 scopus 로고    scopus 로고
    • Diazen-1-ium- 1,2-diolated nitric oxide donor ester prodrugs of 1-(4- methanesulfonylphenyl)-5-aryl-1H-pyrazol-3-carboxylic acids: Synthesis, nitric oxide release studies and anti-inflammatory activities
    • Abdellatif, K.R.A.; Chowdhury, M.A.; Dong, Y.; Knaus, E.E. Diazen-1-ium- 1,2-diolated nitric oxide donor ester prodrugs of 1-(4- methanesulfonylphenyl)-5-aryl-1H-pyrazol-3-carboxylic acids: Synthesis, nitric oxide release studies and anti-inflammatory activities. Bioorg. Med. Chem., 2008, 16, 6528-6534.
    • (2008) Bioorg. Med. Chem , vol.16 , pp. 6528-6534
    • Abdellatif, K.R.A.1    Chowdhury, M.A.2    Dong, Y.3    Knaus, E.E.4
  • 113
    • 48949115102 scopus 로고    scopus 로고
    • Facile synthesis, ex-vivo and in vitro screening of 3-sulfonamide derivative of 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxylic acid piperidin-1-ylamide (SR141716) a potent CB1 receptor antagonist
    • Srivastava, B.K.; Soni, R.; Patel, J.Z.; Jha, S.; Shedage, S.A.; Gandhi, N.; Sairam, K.V.V.M.; Pawar, V.; Sadhwani, N.; Mitra, P.; Jain, M.R.; Patel, P.R. Facile synthesis, ex-vivo and in vitro screening of 3-sulfonamide derivative of 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxylic acid piperidin-1-ylamide (SR141716) a potent CB1 receptor antagonist. Bioorg. Med. Chem. Lett., 2008, 18, 3882-3886.
    • (2008) Bioorg. Med. Chem. Lett , vol.18 , pp. 3882-3886
    • Srivastava, B.K.1    Soni, R.2    Patel, J.Z.3    Jha, S.4    Shedage, S.A.5    Gandhi, N.6    Sairam, K.V.V.M.7    Pawar, V.8    Sadhwani, N.9    Mitra, P.10    Jain, M.R.11    Patel, P.R.12
  • 114
    • 20144379406 scopus 로고    scopus 로고
    • Bioisosteric replacements of the pyrazole moiety of rimonabant: Synthesis, biological properties, and molecular modeling investigations of thiazoles, triazoles, and imidazoles as potent and selective cb1 cannabinoid receptor antagonists
    • Lange, J.H.M.; van Stuivenberg, H.H.; Coolen, H.K.A.C.; Adolfs, T.J.P.; McCreary, A.C.; Keizer, H.G.; Wals, H.C.; Veerman, W.; Borst, A.J.M.; de Looff, W.; Verveer, P.C.; Kruse, C.G. bioisosteric replacements of the pyrazole moiety of rimonabant: synthesis, biological properties, and molecular modeling investigations of thiazoles, triazoles, and imidazoles as potent and selective cb1 cannabinoid receptor antagonists. J. Med. Chem., 2005, 48, 1823-1838.
    • (2005) J. Med. Chem , vol.48 , pp. 1823-1838
    • Lange, J.H.M.1    van Stuivenberg, H.H.2    Coolen, H.K.A.C.3    Adolfs, T.J.P.4    McCreary, A.C.5    Keizer, H.G.6    Wals, H.C.7    Veerman, W.8    Borst, A.J.M.9    de Looff, W.10    Verveer, P.C.11    Kruse, C.G.12
  • 115
    • 33746693727 scopus 로고    scopus 로고
    • Phototransformation of the insecticide fipronil: Identification of novel photoproducts and evidence for an alternative pathway of photodegradation
    • Raveton, M.; Aajoud, A.; Willison, J.C.; Aouadi, H.; Tissut, M.; Ravanel, P. phototransformation of the insecticide fipronil: identification of novel photoproducts and evidence for an alternative pathway of photodegradation. Environ. Sci. Technol., 2006, 40, 4151-4157.
    • (2006) Environ. Sci. Technol , vol.40 , pp. 4151-4157
    • Raveton, M.1    Aajoud, A.2    Willison, J.C.3    Aouadi, H.4    Tissut, M.5    Ravanel, P.6
  • 116
    • 0033784992 scopus 로고    scopus 로고
    • Elucidation of Fipronil Photodegradation pathways
    • Ngim, K.K.; Mabury, S.A.; Crosby, D.G. Elucidation of Fipronil Photodegradation pathways. J. Agric. Food Chem., 2000, 48, 4661-4665.
    • (2000) J. Agric. Food Chem , vol.48 , pp. 4661-4665
    • Ngim, K.K.1    Mabury, S.A.2    Crosby, D.G.3
  • 117
    • 43449106481 scopus 로고    scopus 로고
    • Improved regioselectivity in pyrazole formation through the use of fluorinated alcohols as solvents: Synthesis and biological activity of fluorinated tebufenpyrad analogs
    • Fustero, S.; Román, R.; Sanz-Cervera, J.F.; Simón-Fuentes, A.; Cuñat, A.C.; Villanova, S.; Murguía, M. improved regioselectivity in pyrazole formation through the use of fluorinated alcohols as solvents: synthesis and biological activity of fluorinated tebufenpyrad analogs. J. Org. Chem., 2008, 73, 3523-3529.
    • (2008) J. Org. Chem , vol.73 , pp. 3523-3529
    • Fustero, S.1    Román, R.2    Sanz-Cervera, J.F.3    Simón-Fuentes, A.4    Cuñat, A.C.5    Villanova, S.6    Murguía, M.7
  • 118
    • 0033666768 scopus 로고    scopus 로고
    • Metabolism of Furametpyr. 1. identification of metabolites and in vitro biotransformation in rats and humans
    • Nagahori, H.; Yoshino, H.; Tomigahara, Y.; Isobe, N.; Kaneko, H.; Nakatsuka, I. Metabolism of Furametpyr. 1. identification of metabolites and in vitro biotransformation in rats and humans. J. Agric. Food Chem., 2000, 48, 5754-5759.
    • (2000) J. Agric. Food Chem , vol.48 , pp. 5754-5759
    • Nagahori, H.1    Yoshino, H.2    Tomigahara, Y.3    Isobe, N.4    Kaneko, H.5    Nakatsuka, I.6
  • 121
    • 4143078217 scopus 로고    scopus 로고
    • A study on the synthesis and photophysical performances of some pyrazole and triazole fluorescent brightening agents
    • Wang, X.; Li, W.; Zhang, X.-H.; Liu, D.-Z.; Zhou, X.-Q. A study on the synthesis and photophysical performances of some pyrazole and triazole fluorescent brightening agents. Dyes Pig., 2005, 64(2), 141-146.
    • (2005) Dyes Pig , vol.64 , Issue.2 , pp. 141-146
    • Wang, X.1    Li, W.2    Zhang, X.-H.3    Liu, D.-Z.4    Zhou, X.-Q.5
  • 122
    • 0038729126 scopus 로고    scopus 로고
    • Photoinduced electron transfer reactions of 3H-Pyrazole derivatives. Formation of solvent adduct by specific sensitizer
    • Karatsu, T.; Shiochi, N.; Aono, T.; Miyagawa, N.; Kitamura, A. Photoinduced electron transfer reactions of 3H-Pyrazole derivatives. Formation of solvent adduct by specific sensitizer. Bull. Chem. Soc. Jpn., 2003, 76(6), 1227-1231.
    • (2003) Bull. Chem. Soc. Jpn , vol.76 , Issue.6 , pp. 1227-1231
    • Karatsu, T.1    Shiochi, N.2    Aono, T.3    Miyagawa, N.4    Kitamura, A.5
  • 123
    • 3042567398 scopus 로고    scopus 로고
    • Photoinduced electron transfer reactions of 3,3-Dialkylated 4,5-diphenyl-3H-pyrazoles: A new route to the formation of the solvent adducts
    • Yen, Y.-P.; Huang, T.-M.; Tseng, Y.-P.; Lin, H.-Y.; Lai, C.-C. Photoinduced electron transfer reactions of 3,3-Dialkylated 4,5-diphenyl-3H-pyrazoles: A new route to the formation of the solvent adducts. J. Chin. Chem. Soc., 2004, 51(2), 393-398.
    • (2004) J. Chin. Chem. Soc , vol.51 , Issue.2 , pp. 393-398
    • Yen, Y.-P.1    Huang, T.-M.2    Tseng, Y.-P.3    Lin, H.-Y.4    Lai, C.-C.5
  • 124
    • 33746611878 scopus 로고    scopus 로고
    • Syntheses and properties of new photochromic diarylethene derivatives having a pyrazole unit
    • Pu, S.; Yang, T.; Xu, J.; Chen, B. Syntheses and properties of new photochromic diarylethene derivatives having a pyrazole unit. Tetrahedron Lett., 2006, 47(36), 6473-6477.
    • (2006) Tetrahedron Lett , vol.47 , Issue.36 , pp. 6473-6477
    • Pu, S.1    Yang, T.2    Xu, J.3    Chen, B.4
  • 125
    • 35048850347 scopus 로고    scopus 로고
    • Synthesis and Solid-State Photochromism of 1,3-Diphenyl-4- (2-chlorobenzal)-5-hydroxypyrazole 4- methylthiosemicarbazone
    • Guo, J.; Liu, L.; Liu, G.; Jia, D.; Xie, X. Synthesis and Solid-State Photochromism of 1,3-Diphenyl-4- (2-chlorobenzal)-5-hydroxypyrazole 4- methylthiosemicarbazone. Org. Lett., 2007, 9(20), 3989-3992.
    • (2007) Org. Lett , vol.9 , Issue.20 , pp. 3989-3992
    • Guo, J.1    Liu, L.2    Liu, G.3    Jia, D.4    Xie, X.5
  • 126
    • 11844287668 scopus 로고    scopus 로고
    • Phosphorescent organogels via "Metallophilic" interactions for reversible RGB-color switching
    • Kishimura, A.; Yamashita, T.; Aida, T. Phosphorescent organogels via "Metallophilic" interactions for reversible RGB-color switching. J. Am. Chem. Soc., 2005, 127, 179-183.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 179-183
    • Kishimura, A.1    Yamashita, T.2    Aida, T.3
  • 127
    • 48849102030 scopus 로고    scopus 로고
    • Blueemitting cationic iridium complexes with 2-(1H-Pyrazol-1-yl)pyridine as the ancillary ligand for efficient light-emitting electrochemical cells
    • He, L.; Duan, L.; Qiao, J.; Wang, R.; Wei, P.; Wang, L.; Qiu, Y. Blueemitting cationic iridium complexes with 2-(1H-Pyrazol-1-yl)pyridine as the ancillary ligand for efficient light-emitting electrochemical cells. Adv. Funct. Mater., 2008, 18, 2123-2131.
    • (2008) Adv. Funct. Mater , vol.18 , pp. 2123-2131
    • He, L.1    Duan, L.2    Qiao, J.3    Wang, R.4    Wei, P.5    Wang, L.6    Qiu, Y.7
  • 128
    • 33745684776 scopus 로고    scopus 로고
    • New Efficient bluegreenish electroluminescent materials of 1,3,4-Oxadiazole-based pyrazole DERIVATIVES
    • Chang, E.-M.; Lin, C.J.; Wong, F.F.; Yeh, M.-Y. New Efficient bluegreenish electroluminescent materials of 1,3,4-Oxadiazole-based pyrazole DERIVATIVES. Heterocycles, 2006, 68(4), 733-748.
    • (2006) Heterocycles , vol.68 , Issue.4 , pp. 733-748
    • Chang, E.-M.1    Lin, C.J.2    Wong, F.F.3    Yeh, M.-Y.4
  • 129
    • 0035208217 scopus 로고    scopus 로고
    • Difunctional pyrazole derivatives - key compounds en route to multidentate pyrazolate ligands
    • Röder, J.C.; Meyer, F.; Konrad, M.; Sandhöfner, S.; Kaifer, E.; Pritzkow, H. Difunctional pyrazole derivatives - key compounds en route to multidentate pyrazolate ligands. Eur. J. Org. Chem., 2001, (23), 4479-4487.
    • (2001) Eur. J. Org. Chem , vol.23 , pp. 4479-4487
    • Röder, J.C.1    Meyer, F.2    Konrad, M.3    Sandhöfner, S.4    Kaifer, E.5    Pritzkow, H.6
  • 130
    • 53849090649 scopus 로고    scopus 로고
    • Manganese(II) coordination polymer with ditopic bis(pyrazol-1-yl)borate bridges
    • Morawitz, T.; Bolte, M.; Lerner, H.-W.; Wagner, M. A manganese(II) coordination polymer with ditopic bis(pyrazol-1-yl)borate bridges. Z. Anorg. Allg. Chem., 2008, 634, 1409-1414.
    • (2008) Z. Anorg. Allg. Chem , vol.634 , pp. 1409-1414
    • Morawitz, T.1    Bolte, M.2    Lerner, H.-W.3    Wagner, M.A.4
  • 131
    • 33947402170 scopus 로고    scopus 로고
    • Anion doping as a probe of cooperativity in the molecular spin-crossover compound [FeL2][BF4]2 (L = 2,6-di{pyrazol-1-yl}pyridine)
    • Carbonera, C.; Kilner, C.A.; Létard, J.-F.; Halcrow, M.A. Anion doping as a probe of cooperativity in the molecular spin-crossover compound [FeL2][BF4]2 (L = 2,6-di{pyrazol-1-yl}pyridine). J. Chem. Soc., Dalton Trans., 2007, 1284-1292.
    • (2007) J. Chem. Soc., Dalton Trans , pp. 1284-1292
    • Carbonera, C.1    Kilner, C.A.2    Létard, J.-F.3    Halcrow, M.A.4
  • 132
    • 46149089610 scopus 로고    scopus 로고
    • Selective extraction, separation and speciation of iron in different samples using 4-acetyl-5-methyl-1-phenyl-1H-pyrazole-3- carboxylic acid
    • Saçmaci, Ş.; Kartal, Ş. Selective extraction, separation and speciation of iron in different samples using 4-acetyl-5-methyl-1-phenyl-1H-pyrazole-3- carboxylic acid. Anal. Chim. Acta, 2008, 623, 46-52.
    • (2008) Anal. Chim. Acta , vol.623 , pp. 46-52
    • Saçmaci, S.1    Kartal, S.2
  • 133
    • 51549114661 scopus 로고    scopus 로고
    • Redox-Active p-Quinone-Based Bis(pyrazol-1-yl)methane Ligands: Synthesis and Coordination Behaviour
    • Scheuermann, S.; Kretz, T.; Vitze, H.; Bats, J.W.; Bolte, M.; Lerner, H.-W.; Wagner, M. Redox-Active p-Quinone-Based Bis(pyrazol-1-yl)methane Ligands: Synthesis and Coordination Behaviour. Chem. Eur. J., 2008, 14(8), 2590-2601.
    • (2008) Chem. Eur. J , vol.14 , Issue.8 , pp. 2590-2601
    • Scheuermann, S.1    Kretz, T.2    Vitze, H.3    Bats, J.W.4    Bolte, M.5    Lerner, H.-W.6    Wagner, M.7
  • 134
    • 12344310469 scopus 로고    scopus 로고
    • Multifunctional high-spin biradical pyrazolylbipyridine-bisnitronylnitroxide
    • Zoppellaro, G.; Enkelmann, V.; Geies, A.; Baumgarten, M. A Multifunctional high-spin biradical pyrazolylbipyridine-bisnitronylnitroxide. Org. Lett., 2004, 6(26), 4929-4932.
    • (2004) Org. Lett , vol.6 , Issue.26 , pp. 4929-4932
    • Zoppellaro, G.1    Enkelmann, V.2    Geies, A.3    Baumgarten, M.A.4
  • 135
    • 4544220557 scopus 로고    scopus 로고
    • 2,6- Bis(pyrazolyl)pyridine functionalised with two nitronylnitroxide and iminonitroxide radicals
    • Zoppellaro, G.; Geies, A.; Enkelmann, V.; Baumgarten, M. 2,6- Bis(pyrazolyl)pyridine functionalised with two nitronylnitroxide and iminonitroxide radicals. Eur. J. Org. Chem., 2004, (11), 2367-2374.
    • (2004) Eur. J. Org. Chem , Issue.11 , pp. 2367-2374
    • Zoppellaro, G.1    Geies, A.2    Enkelmann, V.3    Baumgarten, M.4
  • 137
    • 33846610111 scopus 로고    scopus 로고
    • Synthesis and characterization of pyrazolyl-functionalized imidazolium-based ionic liquids and hemilabile (carbene)palladium(ii) complex catalyzed heck reaction
    • Wang, R.; Zeng, Z.; Twamley, B.; Piekarski, M.M.; Shreeve, J.M. synthesis and characterization of pyrazolyl-functionalized imidazolium-based ionic liquids and hemilabile (carbene)palladium(ii) complex catalyzed heck reaction. Eur. J. Org. Chem., 2007, (4), 655-661.
    • (2007) Eur. J. Org. Chem , Issue.4 , pp. 655-661
    • Wang, R.1    Zeng, Z.2    Twamley, B.3    Piekarski, M.M.4    Shreeve, J.M.5
  • 138
    • 24944570649 scopus 로고    scopus 로고
    • New Pyrazolino- and Pyrrolidino[60]fullerenes with Transition-Metal Chelating Pyridine Substituents: Synthesis and Complexation to Ru(II)
    • Modin, J.; Johansson, H.; Grennberg, H. New Pyrazolino- and Pyrrolidino[60]fullerenes with Transition-Metal Chelating Pyridine Substituents: Synthesis and Complexation to Ru(II). Org. Lett., 2005, 7(18), 3977-3979.
    • (2005) Org. Lett , vol.7 , Issue.18 , pp. 3977-3979
    • Modin, J.1    Johansson, H.2    Grennberg, H.3
  • 139
    • 66249139887 scopus 로고    scopus 로고
    • MTO/H2O2/Pyrazole-Mediated NOxidation of meso-Tetraarylporphyrins and -chlorins, and S-Oxidation of a meso-Tetraaryldithiaporphyrin and -chlorin
    • Banerjee, S.; Zeller, M.; Brückner, C. MTO/H2O2/Pyrazole-Mediated NOxidation of meso-Tetraarylporphyrins and -chlorins, and S-Oxidation of a meso-Tetraaryldithiaporphyrin and -chlorin. J. Org. Chem., 2009, 74(11), 4283-4288.
    • (2009) J. Org. Chem , vol.74 , Issue.11 , pp. 4283-4288
    • Banerjee, S.1    Zeller, M.2    Brückner, C.3
  • 140
    • 0033565013 scopus 로고    scopus 로고
    • Role of Aggregates in Claisen acylation reactions of imidazole, Pyrazole, and Thioesters with Lithium Enolates in THF
    • Streitwieser, A.; Leung, S.S.-W.; Kim, Y.-J. Role of Aggregates in Claisen acylation reactions of imidazole, Pyrazole, and Thioesters with Lithium Enolates in THF. Org. Lett., 1999, 1(1), 145-147.
    • (1999) Org. Lett , vol.1 , Issue.1 , pp. 145-147
    • Streitwieser, A.1    Leung, S.S.-W.2    Kim, Y.-J.3
  • 141
    • 18244398634 scopus 로고    scopus 로고
    • Enantioselective Enol lactone synthesis under double catalytic conditions
    • Itoh, K.; Hasegawa, M.; Tanaka, J.; Kanemasa, S. Enantioselective Enol lactone synthesis under double catalytic conditions. Org. Lett., 2005, 7(6), 979-981.
    • (2005) Org. Lett , vol.7 , Issue.6 , pp. 979-981
    • Itoh, K.1    Hasegawa, M.2    Tanaka, J.3    Kanemasa, S.4
  • 142
    • 0035954866 scopus 로고    scopus 로고
    • Efficient introduction of protected guanidines in BOC solid phase peptide synthesis
    • Zhang, Y.; Kennan, A.J. Efficient introduction of protected guanidines in BOC solid phase peptide synthesis. Org. Lett., 2001, 3(15), 2341-2344.
    • (2001) Org. Lett , vol.3 , Issue.15 , pp. 2341-2344
    • Zhang, Y.1    Kennan, A.J.2
  • 143
    • 18544410293 scopus 로고    scopus 로고
    • Optimisation of the Synthesis of guanidines from amines via nitroguanidines Using 3,5-Dimethyl-N-nitro-1Hpyrazole-1-carboxamidine
    • Castillo-Meléndez, J.A.; Golding, B.T. Optimisation of the Synthesis of guanidines from amines via nitroguanidines Using 3,5-Dimethyl-N-nitro-1Hpyrazole-1-carboxamidine. Synthesis, 2004, (10), 1655-1663.
    • (2004) Synthesis , vol.10 , pp. 1655-1663
    • Castillo-Meléndez, J.A.1    Golding, B.T.2
  • 144
  • 145
    • 0037327598 scopus 로고    scopus 로고
    • New bis(chalcones) and their transformation into Bis(pyrazoline) and bis(pyrazole) derivatives
    • Pinto, D.C.G.A.; Silva, A.M.S.; Cavaleiro, J.A.S.; Elguero, J. New bis(chalcones) and their transformation into Bis(pyrazoline) and bis(pyrazole) derivatives. Eur. J. Org. Chem., 2003, (4), 747-755.
    • (2003) Eur. J. Org. Chem , vol.4 , pp. 747-755
    • Pinto, D.C.G.A.1    Silva, A.M.S.2    Cavaleiro, J.A.S.3    Elguero, J.4
  • 146
    • 0043287135 scopus 로고    scopus 로고
    • Oligo(1,4-phenylenepyrazole-3,5-diyl)s
    • Meier, H.; Hormaza, A. Oligo(1,4-phenylenepyrazole-3,5-diyl)s. Eur. J. Org. Chem., 2003, (17), 3372-3377.
    • (2003) Eur. J. Org. Chem , vol.17 , pp. 3372-3377
    • Meier, H.1    Hormaza, A.2
  • 147
    • 35948963968 scopus 로고    scopus 로고
    • SmCl3-Catalyzed C-Acylation of 1,3-Dicarbonyl compounds and malononitrile
    • Shen, Q.; Huang, W.; Wang, J.; Zhou, X. SmCl3-Catalyzed C-Acylation of 1,3-Dicarbonyl compounds and malononitrile. Org. Lett., 2007, 9(22), 4491-4494.
    • (2007) Org. Lett , vol.9 , Issue.22 , pp. 4491-4494
    • Shen, Q.1    Huang, W.2    Wang, J.3    Zhou, X.4
  • 148
    • 33744477678 scopus 로고    scopus 로고
    • Three-Component, one-pot reaction for the combinatorial synthesis of 1,3,4-substituted pyrazoles
    • Xie, F.; Cheng, G.; Hu, Y. Three-Component, one-pot reaction for the combinatorial synthesis of 1,3,4-substituted pyrazoles. J. Comb. Chem., 2006, 8, 286-288.
    • (2006) J. Comb. Chem , vol.8 , pp. 286-288
    • Xie, F.1    Cheng, G.2    Hu, Y.3
  • 149
    • 12344281353 scopus 로고    scopus 로고
    • Synthesis of Pyrazolyl-2-pyrazolines by Treatment of 3-(3-Aryl-3-oxopropenyl)chromen-4-ones with hydrazine and their oxidation to Bis(pyrazoles)
    • Lévai, A.; Silva, A.M.S.; Pinto, D.C.G.A.; Cavaleiro, J.A.S.; Alkorta, I.; Elguero, J.; Jekö, J. Synthesis of Pyrazolyl-2-pyrazolines by Treatment of 3-(3-Aryl-3-oxopropenyl)chromen-4-ones with hydrazine and their oxidation to Bis(pyrazoles). Eur. J. Org. Chem., 2004, (22), 4672-4679.
    • (2004) Eur. J. Org. Chem , vol.22 , pp. 4672-4679
    • Lévai, A.1    Silva, A.M.S.2    Pinto, D.C.G.A.3    Cavaleiro, J.A.S.4    Alkorta, I.5    Elguero, J.6    Jekö, J.7
  • 151
    • 84961980498 scopus 로고    scopus 로고
    • Synthesis of pyrazoles by treatment of 3-Benzylchromones, 3-Benzylflavones and their 4-Thio analogues with hydrazine
    • Lévai, A.; Silva, A.M.S.; Cavaleiro, J.A.S.; Alkorta, I.; Elguero, J.; Jekö, J. Synthesis of pyrazoles by treatment of 3-Benzylchromones, 3-Benzylflavones and their 4-Thio analogues with hydrazine. Eur. J. Org. Chem., 2006, (12), 2825-2832.
    • (2006) Eur. J. Org. Chem , vol.12 , pp. 2825-2832
    • Lévai, A.1    Silva, A.M.S.2    Cavaleiro, J.A.S.3    Alkorta, I.4    Elguero, J.5    Jekö, J.6
  • 152
    • 0034365633 scopus 로고    scopus 로고
    • Syntheses of Pyrazole Iso-C-nucleosides
    • Michalik, D.; Peseke, K. Syntheses of Pyrazole Iso-C-nucleosides. J. Carbohydr Chem., 2000, 19(8), 1049-1057.
    • (2000) J. Carbohydr Chem , vol.19 , Issue.8 , pp. 1049-1057
    • Michalik, D.1    Peseke, K.2
  • 153
    • 0035850191 scopus 로고    scopus 로고
    • Synthesis of derivatives of C-nucleoside analogues using 'push-pull' functionalized monosaccharides
    • Michalik, D.; Feist, H.; Peseke, K. Synthesis of derivatives of C-nucleoside analogues using 'push-pull' functionalized monosaccharides. Carbohydr Res., 2001, 333, 197-201.
    • (2001) Carbohydr Res , vol.333 , pp. 197-201
    • Michalik, D.1    Feist, H.2    Peseke, K.3
  • 155
    • 19944402969 scopus 로고    scopus 로고
    • New hydroxy-pyrazoline intermediates, subtle regioselectivity and relative reaction rate variations observed during acid catalyzed and neutral pyrazole cyclization
    • Norris, T.; Colon-Cruz, R.; Ripin, D.H.B. New hydroxy-pyrazoline intermediates, subtle regioselectivity and relative reaction rate variations observed during acid catalyzed and neutral pyrazole cyclization. Org. Biomol. Chem., 2005, 3, 1844-1849.
    • (2005) Org. Biomol. Chem , vol.3 , pp. 1844-1849
    • Norris, T.1    Colon-Cruz, R.2    Ripin, D.H.B.3
  • 156
    • 0033803272 scopus 로고    scopus 로고
    • The reaction between hydrazines and-dicarbonyl compounds: Proposal for a mechanism
    • Elguero, J.; Rozas, I.; Singh, S.P.; Kumar, D.; Batra, H.; Naithani, R. The reaction between hydrazines and-dicarbonyl compounds: proposal for a mechanism. Can. J. Chem., 2000, 78(8), 1109-1120.
    • (2000) Can. J. Chem , vol.78 , Issue.8 , pp. 1109-1120
    • Elguero, J.1    Rozas, I.2    Singh, S.P.3    Kumar, D.4    Batra, H.5    Naithani, R.6
  • 157
    • 37049090641 scopus 로고
    • Mechanisms of heterocycle ring formation. Part 5. A carbon-13 nuclear magnetic resonance study of pyrazolinone synthesis by the reaction of-ketoesters with substituted hydrazine
    • Katritzky, A.R.; Barczynski, P.; Ostercamp, D.L. Mechanisms of heterocycle ring formation. Part 5. A carbon-13 nuclear magnetic resonance study of pyrazolinone synthesis by the reaction of-ketoesters with substituted hydrazines. J. Chem. Soc., Perkin Trans. II, 1987, (8), 969-975.
    • (1987) J. Chem. Soc., Perkin Trans , vol.II , Issue.8 , pp. 969-975
    • Katritzky, A.R.1    Barczynski, P.2    Ostercamp, D.L.3
  • 158
    • 33747409049 scopus 로고    scopus 로고
    • The reaction of aryl and heteroarylhydrazines with aryl-trifluoromethyl-diketones
    • Singh, S.P.; Kumar, V.; Aggarwal, R.; Elguero, J. The reaction of aryl and heteroarylhydrazines with aryl-trifluoromethyl-diketones. J. Heterocycl. Chem., 2006, 43(4), 1003-1014.
    • (2006) J. Heterocycl. Chem , vol.43 , Issue.4 , pp. 1003-1014
    • Singh, S.P.1    Kumar, V.2    Aggarwal, R.3    Elguero, J.4
  • 159
    • 33644889440 scopus 로고    scopus 로고
    • Regioselectivity in the formation of norbornene-fused pyrazoles: Preparation of 1- substituted derivatives of 4,5,6,7-tetrahydro-1H-4,7-methanoindazole
    • Fernández, F.; Caamaño, O.; García, M.D.; Alkorta, I.; Elguero, J. Regioselectivity in the formation of norbornene-fused pyrazoles: preparation of 1- substituted derivatives of 4,5,6,7-tetrahydro-1H-4,7-methanoindazole. Tetrahedron, 2006, 62, 3362-3369.
    • (2006) Tetrahedron , vol.62 , pp. 3362-3369
    • Fernández, F.1    Caamaño, O.2    García, M.D.3    Alkorta, I.4    Elguero, J.5
  • 161
    • 0000808376 scopus 로고
    • Rearrangements and cyclization-XVII: Mechanism of the formation of 1,2-azoles in reactions of 1,1-diacyclopropanes with hydrazine and hydroxylamine derivatives
    • Zefirov, N.S.; Kozhushkov, S.I.; Kuznetsova, T.S.; Ershov, B.A.; Selivanov, S.I. Rearrangements and cyclization-XVII: Mechanism of the formation of 1,2-azoles in reactions of 1,1-diacyclopropanes with hydrazine and hydroxylamine derivatives. Tetrahedron, 1986, 42(2), 709-713.
    • (1986) Tetrahedron , vol.42 , Issue.2 , pp. 709-713
    • Zefirov, N.S.1    Kozhushkov, S.I.2    Kuznetsova, T.S.3    Ershov, B.A.4    Selivanov, S.I.5
  • 162
    • 0002650309 scopus 로고
    • Isolation of dihydroxypyrazolidine and 5-hydroxy- 2-pyrazoline intermediates in the synthesis of pyrazoles from-diketones and hydrazine
    • Elguero, J.; Yranzo, G.I. Isolation of dihydroxypyrazolidine and 5-hydroxy- 2-pyrazoline intermediates in the synthesis of pyrazoles from-diketones and hydrazine. J. Chem. Res. Synopses, 1990, (4), 120-121.
    • (1990) J. Chem. Res. Synopses , vol.4 , pp. 120-121
    • Elguero, J.1    Yranzo, G.I.2
  • 163
    • 0242487852 scopus 로고    scopus 로고
    • 1,1,1- Trichloro-4,4-diethoxy-3-buten-2-one and its trichloroacetylacetate derivatives: Synthesis and applications in regiospecific preparation of azoles
    • Martins, M.A.P.; Pereira, C.M.P.; Zimmermann, N.E.K.; Moura, S. Sinhorin, A.P.; Cunico, W.; Zanatta, N.; Bonacorso, H.G.; Flores, A.C.F. 1,1,1- Trichloro-4,4-diethoxy-3-buten-2-one and its trichloroacetylacetate derivatives: synthesis and applications in regiospecific preparation of azoles. Synthesis, 2003, (15), 2353-2357.
    • (2003) Synthesis , vol.15 , pp. 2353-2357
    • Martins, M.A.P.1    Pereira, C.M.P.2    Zimmermann, N.E.K.3    Moura, S.4    Sinhorin, A.P.5    Cunico, W.6    Zanatta, N.7    Bonacorso, H.G.8    Flores, A.C.F.9
  • 164
  • 165
    • 33746402789 scopus 로고    scopus 로고
    • Synthesis of new trifluoromethyl-containing 1-(3,5- dialkyl-4-hydroxybenzyl)-pyrazole and -pyrazol-5-one deriatives and their corresponding aroxyls
    • Dinoiu, V.; Lü, J.-M. Synthesis of new trifluoromethyl-containing 1-(3,5- dialkyl-4-hydroxybenzyl)-pyrazole and -pyrazol-5-one deriatives and their corresponding aroxyls. J. Serb. Chem. Soc., 2006, 71(4), 323-330.
    • (2006) J. Serb. Chem. Soc , vol.71 , Issue.4 , pp. 323-330
    • Dinoiu, V.1    Lü, J.-M.2
  • 166
    • 56249118348 scopus 로고    scopus 로고
    • An improved preparation of 3- alkoxypyrazoles
    • Guillou, S.; Bonhomme, F.J.; Janin, Y.L. An improved preparation of 3- alkoxypyrazoles. Synthesis, 2008, (21), 3504-3508.
    • (2008) Synthesis , vol.21 , pp. 3504-3508
    • Guillou, S.1    Bonhomme, F.J.2    Janin, Y.L.3
  • 167
    • 2542589435 scopus 로고    scopus 로고
    • Fully automated Polymer-Assisted synthesis of 1,5-Biaryl pyrazoles
    • Vickerstaffe, E.; Warrington, B.H.; Ladlow, M.; Ley, S.V. Fully automated Polymer-Assisted synthesis of 1,5-Biaryl pyrazoles. J. Comb. Chem., 2004, 6, 332-339.
    • (2004) J. Comb. Chem , vol.6 , pp. 332-339
    • Vickerstaffe, E.1    Warrington, B.H.2    Ladlow, M.3    Ley, S.V.4
  • 168
    • 0037319206 scopus 로고    scopus 로고
    • Microwave-assisted solution-phase synthesis of 1,4,5-Trisubstituted pyrazoles
    • Giacomelli, G.; Porcheddu, A.; Salaris, M.; Taddei, M. Microwave-assisted solution-phase synthesis of 1,4,5-Trisubstituted pyrazoles. Eur. J. Org. Chem., 2003, (3), 537-541.
    • (2003) Eur. J. Org. Chem , vol.3 , pp. 537-541
    • Giacomelli, G.1    Porcheddu, A.2    Salaris, M.3    Taddei, M.4
  • 169
    • 1942521608 scopus 로고    scopus 로고
    • Regioselective rapid analogue syntheses of 1-methyl-3,5-diarylpyrazoles via palladium-catalysed coupling to 3(5)- pyrazolyl nonaflates
    • Bourrain, S.; Ridgill, M.; Collins, I. Regioselective rapid analogue syntheses of 1-methyl-3,5-diarylpyrazoles via palladium-catalysed coupling to 3(5)- pyrazolyl nonaflates. Synlett, 2004, (5), 795-798.
    • (2004) Synlett , vol.5 , pp. 795-798
    • Bourrain, S.1    Ridgill, M.2    Collins, I.3
  • 170
    • 33746105769 scopus 로고    scopus 로고
    • 1,3-Diketones from acid chlorides and Ketones: A rapid and general one-pot synthesis of pyrazoles
    • Heller, S.T.; Natarajan, S.R. 1,3-Diketones from acid chlorides and Ketones: A rapid and general one-pot synthesis of pyrazoles. Org. Lett., 2006, 8(13), 2675-2678.
    • (2006) Org. Lett , vol.8 , Issue.13 , pp. 2675-2678
    • Heller, S.T.1    Natarajan, S.R.2
  • 171
    • 48349083015 scopus 로고    scopus 로고
    • Synthesis of derivatives of pyrazole with chiral substituents at the nitrogen atom
    • Kurkin, A.V.; Utkina, A.A.; Yurovskaya, M.A. Synthesis of derivatives of pyrazole with chiral substituents at the nitrogen atom. Chem. Heterocycl. Comp., 2008, 44(1), 106-108.
    • (2008) Chem. Heterocycl. Comp , vol.44 , Issue.1 , pp. 106-108
    • Kurkin, A.V.1    Utkina, A.A.2    Yurovskaya, M.A.3
  • 172
    • 0034618340 scopus 로고    scopus 로고
    • Versatile and efficient solid-phase syntheses of pyrazoles and isoxazoles
    • Shen, D.-M; Shu, M.; Chapman, K.T. Versatile and efficient solid-phase syntheses of pyrazoles and isoxazoles. Org. Lett., 2000, 2(18), 2789-2792.
    • (2000) Org. Lett , vol.2 , Issue.18 , pp. 2789-2792
    • Shen, D.-M.1    Shu, M.2    Chapman, K.T.3
  • 173
    • 57649126101 scopus 로고    scopus 로고
    • One-pot synthesis of trifluoromethyl-containing pyrazoles via sequential yb(pfo)3-catalyzed three-component reaction and ibx-mediated oxidation
    • Shen, L.; Zhang, J.; Cao, S.; Yu, J.; Liu, N.; Wu, J.; Qian, X. one-pot synthesis of trifluoromethyl-containing pyrazoles via sequential yb(pfo)3-catalyzed three-component reaction and ibx-mediated oxidation. Synlett, 2008, (19), 3058-3062.
    • (2008) Synlett , vol.19 , pp. 3058-3062
    • Shen, L.1    Zhang, J.2    Cao, S.3    Yu, J.4    Liu, N.5    Wu, J.6    Qian, X.7
  • 174
    • 45749146306 scopus 로고    scopus 로고
    • Ytterbium(III) Perfluorooctanoate catalyzed one-pot, three-component synthesis of fully substituted pyrazoles under solvent-free conditions
    • Shen, L.; Cao, S.; Liu, N.; Wu, J.; Zhu, L.; Qian, X. Ytterbium(III) Perfluorooctanoate catalyzed one-pot, three-component synthesis of fully substituted pyrazoles under solvent-free conditions. Synlett, 2008, (9), 1341-1344.
    • (2008) Synlett , vol.9 , pp. 1341-1344
    • Shen, L.1    Cao, S.2    Liu, N.3    Wu, J.4    Zhu, L.5    Qian, X.6
  • 175
    • 28844481893 scopus 로고    scopus 로고
    • Layered zirconium sulfophenyl phosphonate as heterogeneous catalyst in the synthesis of pyrazoles and 4,5,6,7-Tetrahydro-1(2)Hindazoles
    • Curini, M.; Rosati, O.; Campagna, V.; Montanari, F.; Cravotto, G.; Boccalini, M. Layered zirconium sulfophenyl phosphonate as heterogeneous catalyst in the synthesis of pyrazoles and 4,5,6,7-Tetrahydro-1(2)Hindazoles. Synlett, 2005, (19), 2927-2930.
    • (2005) Synlett , vol.19 , pp. 2927-2930
    • Curini, M.1    Rosati, O.2    Campagna, V.3    Montanari, F.4    Cravotto, G.5    Boccalini, M.6
  • 176
    • 77955361025 scopus 로고    scopus 로고
    • The preparation of substituted pyrazoles from-Dibromo-enones by a Tandem Condensation/Suzuki-Miyaura cross-coupling Process
    • Beltrán-Rodil, S.; Edwards, M.G.; Pugh, D.S.; Reid, M.; Taylor, R.J.K. The preparation of substituted pyrazoles from-Dibromo-enones by a Tandem Condensation/Suzuki-Miyaura cross-coupling Process. Synlett, 2010, (4), 602-606.
    • (2010) Synlett , vol.4 , pp. 602-606
    • Beltrán-Rodil, S.1    Edwards, M.G.2    Pugh, D.S.3    Reid, M.4    Taylor, R.J.K.5
  • 177
    • 33745612700 scopus 로고    scopus 로고
    • A general method for the preparation of 3-acyl-4- cyano-5-amino-pyrazoles
    • Ge, M.; Cline, E.; Yang, L. A general method for the preparation of 3-acyl-4- cyano-5-amino-pyrazoles. Tetrahedron Lett., 2006, 47(32), 5797-5799.
    • (2006) Tetrahedron Lett , vol.47 , Issue.32 , pp. 5797-5799
    • Ge, M.1    Cline, E.2    Yang, L.3
  • 178
    • 0035148326 scopus 로고    scopus 로고
    • Microwave Assisted Synthesis of 1-Aryl-3-dimethylaminoprop-2-enones: A Simple and Rapid Access to 3(5)-Arylpyrazoles
    • Pleier, A.-K.; Glas, H.; Grosche, M.; Sirsch, P.; Thiel, W.R. Microwave Assisted Synthesis of 1-Aryl-3-dimethylaminoprop-2-enones: A Simple and Rapid Access to 3(5)-Arylpyrazoles. Synthesis, 2001, (1), 55-62.
    • (2001) Synthesis , vol.1 , pp. 55-62
    • Pleier, A.-K.1    Glas, H.2    Grosche, M.3    Sirsch, P.4    Thiel, W.R.5
  • 179
    • 3142775570 scopus 로고    scopus 로고
    • Montmorillonite KSF clay-promoted synthesis of enantiomerically pure 5- substituted pyrazoles from 2,3-dihydro-4H-pyran-4-ones
    • Yadav, J.S.; Subba Reddy, B.V.; Srinivas, M.; Prabhakar, A.; Jagadeesh, B. Montmorillonite KSF clay-promoted synthesis of enantiomerically pure 5- substituted pyrazoles from 2,3-dihydro-4H-pyran-4-ones. Tetrahedron Lett., 2004, 45(31), 6033-6036.
    • (2004) Tetrahedron Lett , vol.45 , Issue.31 , pp. 6033-6036
    • Yadav, J.S.1    Subba, R.B.V.2    Srinivas, M.3    Prabhakar, A.4    Jagadeesh, B.5
  • 180
    • 5644285399 scopus 로고    scopus 로고
    • Rapid and efficient synthesis of optically active pyrazoles under solvent-free conditions
    • Yadav, J.S.; Reddy, B.V.S.; Satheesh, G.; Naga Lakshmi, P.; Kiran Kumarb, S.; Kunwar, A.C. Rapid and efficient synthesis of optically active pyrazoles under solvent-free conditions. Tetrahedron Lett., 2004, 45(46), 8587-8590.
    • (2004) Tetrahedron Lett , vol.45 , Issue.46 , pp. 8587-8590
    • Yadav, J.S.1    Reddy, B.V.S.2    Satheesh, G.3    Naga, L.P.4    Kiran, K.S.5    Kunwar, A.C.6
  • 181
    • 0035812782 scopus 로고    scopus 로고
    • Regioselective synthesis of polysubstituted pyrazoles and isoxazoles
    • Katritzky, A.R.; Wang, M.; Zhang, S.; Voronkov, M.V.; Steel, P.J. Regioselective synthesis of polysubstituted pyrazoles and isoxazoles. J. Org. Chem., 2001, 66, 6787-6791.
    • (2001) J. Org. Chem , vol.66 , pp. 6787-6791
    • Katritzky, A.R.1    Wang, M.2    Zhang, S.3    Voronkov, M.V.4    Steel, P.J.5
  • 182
    • 28044473878 scopus 로고    scopus 로고
    • Regioselective Synthesis of 1-Aryl-3,4-substituted/annulated-5-(methylthio)pyrazoles and 1- Aryl-3-(methylthio)-4,5-substituted/annulated Pyrazoles
    • Peruncheralathan, S.; Khan, T.A.; Ila, H.; Junjappa, H. Regioselective Synthesis of 1-Aryl-3,4-substituted/annulated-5-(methylthio)pyrazoles and 1- Aryl-3-(methylthio)-4,5-substituted/annulated Pyrazoles. J. Org. Chem., 2005, 70, 10030-10035.
    • (2005) J. Org. Chem , vol.70 , pp. 10030-10035
    • Peruncheralathan, S.1    Khan, T.A.2    Ila, H.3    Junjappa, H.4
  • 183
    • 27744591612 scopus 로고    scopus 로고
    • Highly regioselective synthesis of 1-Aryl-3 (or 5)-alkyl/aryl-5 (or 3)-(N-cycloamino)pyrazoles
    • Peruncheralathan, S.; Yadav, A.K.; Ila, H.; Junjappa, H. Highly regioselective synthesis of 1-Aryl-3 (or 5)-alkyl/aryl-5 (or 3)-(N-cycloamino)pyrazoles. J. Org. Chem., 2005, 70, 9644-9647.
    • (2005) J. Org. Chem , vol.70 , pp. 9644-9647
    • Peruncheralathan, S.1    Yadav, A.K.2    Ila, H.3    Junjappa, H.4
  • 184
    • 2542609193 scopus 로고    scopus 로고
    • Hydroxyalkynyl Ketones as useful scaffolds for the preparation of combinatorial libraries of furans, isoxazoles and pyrazoles
    • Sauers, R.R.; van Arnum, S.D. -Hydroxyalkynyl Ketones as useful scaffolds for the preparation of combinatorial libraries of furans, isoxazoles and pyrazoles. J. Comb. Chem., 2004, 6, 350-355.
    • (2004) J. Comb. Chem , vol.6 , pp. 350-355
    • Sauers, R.R.1    van Arnum, S.D.2
  • 185
    • 28244440942 scopus 로고    scopus 로고
    • Synthesis of substituted 1-C-Phenyl-D-tetritols and 1-C-(1H-Pyrazol-4-yl)- D-tetritols by ring transformation of 2-Formylglycals
    • Montero, A.; Michalik, M.; Feist, H.; Reinke, H.; Rudloff, I.; Peseke, K. Synthesis of substituted 1-C-Phenyl-D-tetritols and 1-C-(1H-Pyrazol-4-yl)- D-tetritols by ring transformation of 2-Formylglycals. J. Carbohydr. Chem., 2004, 23(5), 313-324.
    • (2004) J. Carbohydr. Chem , vol.23 , Issue.5 , pp. 313-324
    • Montero, A.1    Michalik, M.2    Feist, H.3    Reinke, H.4    Rudloff, I.5    Peseke, K.6
  • 186
    • 46749133810 scopus 로고    scopus 로고
    • An improved synthesis of pyrimidine- and pyrazole-based acyclo-C-nucleosides as carbohybrids
    • Sagar, R.; Kim, M.-J.; Park, S.B. An improved synthesis of pyrimidine- and pyrazole-based acyclo-C-nucleosides as carbohybrids. Tetrahedron Lett., 2008, 49, 5080-5083.
    • (2008) Tetrahedron Lett , vol.49 , pp. 5080-5083
    • Sagar, R.1    Kim, M.-J.2    Park, S.B.3
  • 187
    • 0035136831 scopus 로고    scopus 로고
    • Efficient synthesis of 4-Fluoro-5-(perfluoroalkyl)pyrazoles from organofluorosilicon building blocks
    • Bouillon, J.P.; Didier, B.; Dondy, B.; Doussot, P.; Plantier-Royon, R.; Portella, C. Efficient synthesis of 4-Fluoro-5-(perfluoroalkyl)pyrazoles from organofluorosilicon building blocks. Eur. J. Org. Chem., 2001, (1), 187-192.
    • (2001) Eur. J. Org. Chem , vol.1 , pp. 187-192
    • Bouillon, J.P.1    Didier, B.2    Dondy, B.3    Doussot, P.4    Plantier-Royon, R.5    Portella, C.6
  • 188
    • 34347344028 scopus 로고    scopus 로고
    • Synthesis of Pyrazoles by a one-pot tandem cyclization-dehydrogenation approach on Pd/C/K- 10 catalyst
    • Landge, S.M.; Schmidt, A.; Outerbridge, V.; Török, B. Synthesis of Pyrazoles by a one-pot tandem cyclization-dehydrogenation approach on Pd/C/K- 10 catalyst. Synlett, 2007, (10), 1600-1604.
    • (2007) Synlett , vol.10 , pp. 1600-1604
    • Landge, S.M.1    Schmidt, A.2    Outerbridge, V.3    Török, B.4
  • 189
    • 33646797446 scopus 로고    scopus 로고
    • Palladium-catalyzed C-N bond formation: Synthesis of 1-aryl-1H-pyrazoles from β-bromovinyl aldehydes and arylhydrazines
    • Cho, C.S.; Patel, D.P. Palladium-catalyzed C-N bond formation: synthesis of 1-aryl-1H-pyrazoles from β-bromovinyl aldehydes and arylhydrazines. Tetrahedron, 2006, 62(26), 6388-6391.
    • (2006) Tetrahedron , vol.62 , Issue.26 , pp. 6388-6391
    • Cho, C.S.1    Patel, D.P.2
  • 190
    • 14644442895 scopus 로고    scopus 로고
    • Synthesis of 5- Hydroxy- and 5-Amino-1-tosyl-5-phenyl-3-(2-arylvinyl)-4,5--dihydropyrazoles
    • Kuźmenok, N.M.; Kovaĺchuk, T.A.; Zvonok, A.M. Synthesis of 5- Hydroxy- and 5-Amino-1-tosyl-5-phenyl-3-(2-arylvinyl)-4,5--dihydropyrazoles. Synlett, 2005, (3), 485-486.
    • (2005) Synlett , vol.3 , pp. 485-486
    • Kuźmenok, N.M.1    Kovaĺchuk, T.A.2    Zvonok, A.3
  • 191
    • 70350510129 scopus 로고    scopus 로고
    • The chemistry of-ditosyloxyketones: New and convenient route for the synthesis of 1,4,5-trisubstituted pyrazoles from-chalcone ditosylates
    • Prakash, O.; Sharma, D.; Kamal, R.; Kumar, R.; Nair, R.R. The chemistry of-ditosyloxyketones: new and convenient route for the synthesis of 1,4,5-trisubstituted pyrazoles from-chalcone ditosylates. Tetrahedron, 2009, 65(49), 10175-10181.
    • (2009) Tetrahedron , vol.65 , Issue.49 , pp. 10175-10181
    • Prakash, O.1    Sharma, D.2    Kamal, R.3    Kumar, R.4    Nair, R.R.5
  • 192
    • 28844457259 scopus 로고    scopus 로고
    • Facile preparation of allyl amines and pyrazoles by hydrazinolysis of 2-ketoaziridines
    • Chen, G.; Sasaki, M.; Yudin, A.K. Facile preparation of allyl amines and pyrazoles by hydrazinolysis of 2-ketoaziridines. Tetrahedron Lett., 2006, 47(3), 255-259.
    • (2006) Tetrahedron Lett , vol.47 , Issue.3 , pp. 255-259
    • Chen, G.1    Sasaki, M.2    Yudin, A.K.3
  • 193
    • 0035251041 scopus 로고    scopus 로고
    • Scope and limitations in the regioselective synthesis of 1,3,5- trisubstituted pyrazoles from -Amino Enones and hydrazine derivatives. 13C-chemical shift prediction rules for 1,3,5-Trisubstituted pyrazoles
    • Alberola, A.; Calvo Bleye, L.; González-Ortega, A.; Sábada, M.L.; Sañudo, M.C. Scope and limitations in the regioselective synthesis of 1,3,5- trisubstituted pyrazoles from -Amino Enones and hydrazine derivatives. 13C-chemical shift prediction rules for 1,3,5-Trisubstituted pyrazoles. Heterocycles, 2001, 55(2), 331-351.
    • (2001) Heterocycles , vol.55 , Issue.2 , pp. 331-351
    • Alberola, A.1    Calvo, B.L.2    González-Ortega, A.3    Sábada, M.L.4    Sañudo, M.C.5
  • 194
    • 28844470382 scopus 로고    scopus 로고
    • Silylated-enaminones as precursors in the regioselective synthesis of silyl pyrazoles
    • Calle, M.; Calvo, L.A.; González-Ortega, A.; González-Nogal, A.M. Silylated-enaminones as precursors in the regioselective synthesis of silyl pyrazoles. Tetrahedron, 2006, 62, 611-618.
    • (2006) Tetrahedron , vol.62 , pp. 611-618
    • Calle, M.1    Calvo, L.A.2    González-Ortega, A.3    González-Nogal, A.M.4
  • 195
    • 27644584128 scopus 로고    scopus 로고
    • A convenient approach to the synthesis of -heterocyclic amino acids from carboxy lactams through ring-chain transformation; part 1: Synthesis of (2s)-/(2r)-2- amino-4-(1-aryl-/1,5-diaryl-1h-pyrazol-3-yl)butyric acid
    • Singh, R.K.; Sinha, N.; Jain, S.; Salman, M.; Naqvi, F.; Anand, N. a convenient approach to the synthesis of -heterocyclic amino acids from carboxy lactams through ring-chain transformation; part 1: synthesis of (2s)-/(2r)-2- amino-4-(1-aryl-/1,5-diaryl-1h-pyrazol-3-yl)butyric acid. Synthesis, 2005, (16), 2765-2771.
    • (2005) Synthesis , vol.16 , pp. 2765-2771
    • Singh, R.K.1    Sinha, N.2    Jain, S.3    Salman, M.4    Naqvi, F.5    Anand, N.6
  • 196
    • 27644552250 scopus 로고    scopus 로고
    • Expeditious Solidphase synthesis of pyrazoledicarboxylic acid derivatives by functionalization of resin-bound cyanoformate
    • Morelli, C.F.; Saladino, A.; Speranza, G.; Manitto, P. Expeditious Solidphase synthesis of pyrazoledicarboxylic acid derivatives by functionalization of resin-bound cyanoformate. Eur. J. Org. Chem., 2005, (21), 4621-4627.
    • (2005) Eur. J. Org. Chem , vol.21 , pp. 4621-4627
    • Morelli, C.F.1    Saladino, A.2    Speranza, G.3    Manitto, P.4
  • 197
    • 0141742132 scopus 로고    scopus 로고
    • Toward safer methodologies for the synthesis of polyheterocyclic systems: Intramolecular arylation of arenes under mizoroki-heck reaction conditions
    • Hernández, S.; SanMartin, R.; Tellitu, I.; Domínguez, E. Toward safer methodologies for the synthesis of polyheterocyclic systems: intramolecular arylation of arenes under mizoroki heck reaction conditions. Org. Lett., 2003, 5(7), 1095-1098.
    • (2003) Org. Lett , vol.5 , Issue.7 , pp. 1095-1098
    • Hernández, S.1    Sanmartin, R.2    Tellitu, I.3    Domínguez, E.4
  • 198
    • 33746868887 scopus 로고    scopus 로고
    • Synthesis of N-Methoxy-N-methyl-?-enaminoketoesters: New synthetic precursors for the regioselective synthesis of heterocyclic compounds
    • Persson, T.; Nielsen, J. Synthesis of N-Methoxy-N-methyl-?-enaminoketoesters: new synthetic precursors for the regioselective synthesis of heterocyclic compounds. Org. Lett., 2006, 8(15), 3219-3222.
    • (2006) Org. Lett , vol.8 , Issue.15 , pp. 3219-3222
    • Persson, T.1    Nielsen, J.2
  • 199
    • 51549101998 scopus 로고    scopus 로고
    • Room temperature ICl-Induced Dehydration/ Iodination of 1-Acyl-5-hydroxy-4,5-dihydro-1H-pyrazoles. A selective route to substituted 1-Acyl-4-iodo-1H-pyrazoles
    • Waldo, J.P.; Mehta, S.; Larock, R.C. Room temperature ICl-Induced Dehydration/ Iodination of 1-Acyl-5-hydroxy-4,5-dihydro-1H-pyrazoles. A selective route to substituted 1-Acyl-4-iodo-1H-pyrazoles. J. Org. Chem., 2008, 73, 6666-6670.
    • (2008) J. Org. Chem , vol.73 , pp. 6666-6670
    • Waldo, J.P.1    Mehta, S.2    Larock, R.C.3
  • 200
    • 0142027266 scopus 로고    scopus 로고
    • Synthesis of multi-substituted pyrazoles utilizing the N-Alkylated 3- Hydroxy-3-propargyl- or allenylisoindolines
    • Choi, Y.H.; Kim, K.S.; Lee, S.; Jeong, T.-S.; Lee, H.-Y.; Kim, Y.H.; Lee, W.S. Synthesis of multi-substituted pyrazoles utilizing the N-Alkylated 3- Hydroxy-3-propargyl- or allenylisoindolines. Heterocycles, 2003, 60(11), 2499-2510.
    • (2003) Heterocycles , vol.60 , Issue.11 , pp. 2499-2510
    • Choi, Y.H.1    Kim, K.S.2    Lee, S.3    Jeong, T.-S.4    Lee, H.-Y.5    Kim, Y.H.6    Lee, W.S.7
  • 201
    • 0037463787 scopus 로고    scopus 로고
    • Practical routes to diacetylenic ketones and their application for the preparation of alkynyl substituted pyridines, pyrimidines and pyrazoles
    • Adamo, M.F.A.; Adlington, R.M.; Baldwin, J.E.; Pritchard, G.J.; Rathmella, R.E. Practical routes to diacetylenic ketones and their application for the preparation of alkynyl substituted pyridines, pyrimidines and pyrazoles. Tetrahedron, 2003, 59(13), 2197-2205.
    • (2003) Tetrahedron , vol.59 , Issue.13 , pp. 2197-2205
    • Adamo, M.F.A.1    Adlington, R.M.2    Baldwin, J.E.3    Pritchard, G.J.4    Rathmella, R.E.5
  • 202
    • 26444497881 scopus 로고    scopus 로고
    • One-pot construction of pyrazoles and isoxazoles with Palladium-Catalyzed four-component coupling
    • Ahmed, M.S.M.; Kobayashi, K.; Mori, A. One-pot construction of pyrazoles and isoxazoles with Palladium-Catalyzed four-component coupling. Org. Lett., 2005, 7(20), 4487-4489.
    • (2005) Org. Lett , vol.7 , Issue.20 , pp. 4487-4489
    • Ahmed, M.S.M.1    Kobayashi, K.2    Mori, A.3
  • 204
    • 52249112156 scopus 로고    scopus 로고
    • Regioselective three-component synthesis of highly fluorescent 1,3,5-Trisubstituted pyrazoles
    • Willy, B.; Müller, T.J.J. Regioselective three-component synthesis of highly fluorescent 1,3,5-Trisubstituted pyrazoles. Eur. J. Org. Chem., 2008, (24), 4157-4168.
    • (2008) Eur. J. Org. Chem , vol.24 , pp. 4157-4168
    • Willy, B.1    Müller, T.J.J.2
  • 205
    • 43349104749 scopus 로고    scopus 로고
    • Onepot three-component synthesis of pyrazoles through a tandem couplingcyclocondensation sequence
    • Liu, H.-L.; Jiang, H.-F.; Zhang, M.; Yao, W.-J.; Zhu, Q.-H.; Tang, Z. Onepot three-component synthesis of pyrazoles through a tandem couplingcyclocondensation sequence. Tetrahedron Lett., 2008, 49, 3805-3809.
    • (2008) Tetrahedron Lett , vol.49 , pp. 3805-3809
    • Liu, H.-L.1    Jiang, H.-F.2    Zhang, M.3    Yao, W.-J.4    Zhu, Q.-H.5    Tang, Z.6
  • 206
    • 33947729953 scopus 로고    scopus 로고
    • Regioselective microwave-assisted synthesis of substituted pyrazoles from ethynyl ketones
    • Bagley, M.C.; Lubinu, M.C.; Mason, C. Regioselective microwave-assisted synthesis of substituted pyrazoles from ethynyl ketones. Synlett, 2007, (5), 704-708.
    • (2007) Synlett , vol.5 , pp. 704-708
    • Bagley, M.C.1    Lubinu, M.C.2    Mason, C.3
  • 207
    • 58149341296 scopus 로고    scopus 로고
    • A novel one-pot, threecomponent synthesis of dialkyl 5-(alkylamino)-1-aryl-1h-pyrazole-3,4-dicarboxylates
    • Adib, M.; Mohammadi, B.; Reza Bijanzadeh, H. A novel one-pot, threecomponent synthesis of dialkyl 5-(alkylamino)-1-aryl-1h-pyrazole-3,4-dicarboxylates. Synlett, 2008, (20), 3180-3182.
    • (2008) Synlett , vol.20 , pp. 3180-3182
    • Adib, M.1    Mohammadi, B.2    Reza, B.H.3
  • 208
    • 35848958616 scopus 로고    scopus 로고
    • Palladium-catalyzed alkynylcarbonylation of Aryl Iodides with the use of Mo(CO)6 in the presence of tBu3P ligand
    • Iizuka, M.; Kondo, Y. Palladium-catalyzed alkynylcarbonylation of Aryl Iodides with the use of Mo(CO)6 in the presence of tBu3P ligand. Eur. J. Org. Chem., 2007, (31), 5180-5182.
    • (2007) Eur. J. Org. Chem , vol.31 , pp. 5180-5182
    • Iizuka, M.1    Kondo, Y.2
  • 209
    • 48849090860 scopus 로고    scopus 로고
    • Zinc-Catalyzed synthesis of pyrazolines and pyrazoles via hydrohydrazination
    • Alex, K.; Tillack, A.; Schwarz, N.; Beller, M. Zinc-Catalyzed synthesis of pyrazolines and pyrazoles via hydrohydrazination. Org. Lett., 2008, 10(12), 2377-2379.
    • (2008) Org. Lett , vol.10 , Issue.12 , pp. 2377-2379
    • Alex, K.1    Tillack, A.2    Schwarz, N.3    Beller, M.4
  • 210
    • 52749097629 scopus 로고    scopus 로고
    • A convenient synthesis of novel 7- phosphonylbenzyl-2-substituted pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]- pyrimidine derivatives
    • Xiao, L.-X.; Li, K.; Meng, L.; Shi, D.-Q. A convenient synthesis of novel 7- phosphonylbenzyl-2-substituted pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]- pyrimidine derivatives. Heteroatom Chem., 2008, 19(6), 634-638.
    • (2008) Heteroatom Chem , vol.19 , Issue.6 , pp. 634-638
    • Xiao, L.-X.1    Li, K.2    Meng, L.3    Shi, D.-Q.4
  • 211
    • 13544271031 scopus 로고    scopus 로고
    • Solid-phase synthesis of 5-amino-1-(Substituted Thiocarbamoyl)pyrazole and 1,2,4- triazole derivatives via dithiocarbazate linker
    • Hwang, J.Y.; Choi, H.-S.; Lee, D.-H.; Yoo, S.-E.; Gong, Y.D. Solid-phase synthesis of 5-amino-1-(Substituted Thiocarbamoyl)pyrazole and 1,2,4- triazole derivatives via dithiocarbazate linker. J. Comb. Chem., 2005, 7, 136-141.
    • (2005) J. Comb. Chem , vol.7 , pp. 136-141
    • Hwang, J.Y.1    Choi, H.-S.2    Lee, D.-H.3    Yoo, S.-E.4    Gong, Y.D.5
  • 212
    • 34250342161 scopus 로고    scopus 로고
    • Two new syntheses of a 4-aminopyrazole: Condensation of an N-substituted vinamidinium salt with a functionalized hydrazine
    • Hill, G.B.; Mortlock, A.A. Two new syntheses of a 4-aminopyrazole: condensation of an N-substituted vinamidinium salt with a functionalized hydrazine. Synthesis, 2007, (11), 1697-1701.
    • (2007) Synthesis , vol.11 , pp. 1697-1701
    • Hill, G.B.1    Mortlock, A.A.2
  • 214
    • 31144467616 scopus 로고    scopus 로고
    • Aqueous N-Heterocyclization of primary amines and hydrazines with dihalides: Microwave-assisted syntheses of Nazacycloalkanes, isoindole, pyrazole, pyrazolidine, and phthalazine derivatives
    • Ju, Y.; Varma, R.S. Aqueous N-Heterocyclization of primary amines and hydrazines with dihalides: microwave-assisted syntheses of Nazacycloalkanes, isoindole, pyrazole, pyrazolidine, and phthalazine derivatives. J. Org. Chem., 2006, 71, 135-141.
    • (2006) J. Org. Chem , vol.71 , pp. 135-141
    • Ju, Y.1    Varma, R.S.2
  • 215
    • 0033020246 scopus 로고    scopus 로고
    • Tosylhydrazono phosphonates in organic synthesis. An Unambiguous entry to polysubstituted pyrazoles
    • Almirante, N.; Benicchio, A.; Cerri, A.; Fedrizzi, G.; Marazzi, G.; Santagostino, M.-Tosylhydrazono phosphonates in organic synthesis. An Unambiguous entry to polysubstituted pyrazoles. Synlett, 1999, (3), 299-302.
    • (1999) Synlett , vol.3 , pp. 299-302
    • Almirante, N.1    Benicchio, A.2    Cerri, A.3    Fedrizzi, G.4    Marazzi, G.5    Santagostino, M.6
  • 216
    • 0034029615 scopus 로고    scopus 로고
    • A New Straightforward Formation of aminopyrazoles from isocyanides
    • Atlan, V.; Buron, C.; El Kaïm, L. A New Straightforward Formation of aminopyrazoles from isocyanides. Synlett, 2000, (4), 489-490.
    • (2000) Synlett , vol.4 , pp. 489-490
    • Atlan, V.1    Buron, C.2    El Kaïm, L.3
  • 217
    • 33745386374 scopus 로고    scopus 로고
    • A concise synthesis of Trifluoromethyl-substituted 4-aryloxy pyrazoles
    • Jones, L.H.; Mowbray, C. A concise synthesis of Trifluoromethyl-substituted 4-aryloxy pyrazoles. Synlett, 2006, (9), 1404-1406.
    • (2006) Synlett , vol.9 , pp. 1404-1406
    • Jones, L.H.1    Mowbray, C.2
  • 218
    • 0034008049 scopus 로고    scopus 로고
    • Trichloroacylhydrazones: New straightforward preparation of pyrazoles from keto esters
    • El Kaim, L.; Lacroix, S. Trichloroacylhydrazones: New straightforward preparation of pyrazoles from keto esters. Synlett, 2000, (3), 353-354.
    • (2000) Synlett , vol.3 , pp. 353-354
    • El Kaim, L.1    Lacroix, S.2
  • 219
    • 33747214078 scopus 로고    scopus 로고
    • Reaction of N-Monosubstituted hydrazones with Nitroolefins: A novel regioselective pyrazole synthesis
    • Deng, X.; Mani, N.S. Reaction of N-Monosubstituted hydrazones with Nitroolefins: A novel regioselective pyrazole synthesis. Org. Lett., 2006, 8(16), 3505-3508.
    • (2006) Org. Lett , vol.8 , Issue.16 , pp. 3505-3508
    • Deng, X.1    Mani, N.S.2
  • 220
    • 41849086318 scopus 로고    scopus 로고
    • Regioselective Synthesis of 1,3,5-Tri- and 1,3,4,5- Tetrasubstituted Pyrazoles from N-arylhydrazones and nitroolefins
    • Deng, X.; Mani, N.S. Regioselective Synthesis of 1,3,5-Tri- and 1,3,4,5- Tetrasubstituted Pyrazoles from N-arylhydrazones and nitroolefins. J. Org. Chem., 2008, 73, 2412-2415.
    • (2008) J. Org. Chem , vol.73 , pp. 2412-2415
    • Deng, X.1    Mani, N.S.2
  • 221
    • 8744252642 scopus 로고    scopus 로고
    • A mild procedure for the preparation of 3-Aryl-4-formylpyrazoles
    • De Luca, L.; Giacomelli, G.; Masala, S.; Porcheddu, A. A mild procedure for the preparation of 3-Aryl-4-formylpyrazoles. Synlett, 2004, (13), 2299-2302.
    • (2004) Synlett , vol.13 , pp. 2299-2302
    • de Luca, L.1    Giacomelli, G.2    Masala, S.3    Porcheddu, A.4
  • 222
    • 38349141840 scopus 로고    scopus 로고
    • Synthesis of pyrazole- 3-carboxylates and pyrazole-1,5-dicarboxylates by one-pot cyclization of hydrazone dianions with diethyl oxalate
    • Dang, T.T.; Dang, T.T.; Fischer, C.; Görls, H.; Langer, P. Synthesis of pyrazole- 3-carboxylates and pyrazole-1,5-dicarboxylates by one-pot cyclization of hydrazone dianions with diethyl oxalate. Tetrahedron, 2008, 64(9), 2207-2215.
    • (2008) Tetrahedron , vol.64 , Issue.9 , pp. 2207-2215
    • Dang, T.T.1    Dang, T.T.2    Fischer, C.3    Görls, H.4    Langer, P.5
  • 223
    • 34247097022 scopus 로고    scopus 로고
    • One-pot synthesis of pyrazole-5- carboxylates by cyclization of hydrazone 1,4-dianions with diethyl oxalate
    • Dang, T. T.; Dang, T.T.; Langer, P. One-pot synthesis of pyrazole-5- carboxylates by cyclization of hydrazone 1,4-dianions with diethyl oxalate. Tetrahedron Lett., 2007, 48(20), 3591-3593.
    • (2007) Tetrahedron Lett , vol.48 , Issue.20 , pp. 3591-3593
    • Dang, T.T.1    Dang, T.T.2    Langer, P.3
  • 224
    • 0036843335 scopus 로고    scopus 로고
    • Coupling of Heteroaryldiazonium tetrafluoroborates with 1,3-dicarbonyl compounds-regioselective synthesis of Alkyl 1-Heteroaryl-4-hydroxy-1H-pyrazole-3-carboxylates
    • Renik, S.; Svete, J.; Stanovnik, B. Coupling of Heteroaryldiazonium tetrafluoroborates with 1,3-dicarbonyl compounds-regioselective synthesis of Alkyl 1-Heteroaryl-4-hydroxy-1H-pyrazole-3-carboxylates. Heterocycles, 2002, 57(11), 2091-2106.
    • (2002) Heterocycles , vol.57 , Issue.11 , pp. 2091-2106
    • Renik, S.1    Svete, J.2    Stanovnik, B.3
  • 225
    • 0037711833 scopus 로고    scopus 로고
    • Synthesis of aminopyrazoles from-Oxoketene O,NAcetals using montmorillonite k-10/ultrasound
    • Braibante, M.E.F.; Braibante, H.T.S.; da Roza, J.K.; Henriques, D.M.; de Carvalho Tavares, L. Synthesis of aminopyrazoles from-Oxoketene O,NAcetals using montmorillonite k-10/ultrasound. Synthesis, 2003, (8), 1160-1162.
    • (2003) Synthesis , vol.8 , pp. 1160-1162
    • Braibante, M.E.F.1    Braibante, H.T.S.2    da Roza, J.K.3    Henriques, D.M.4    de Carvalho, T.L.5
  • 227
    • 47049104389 scopus 로고    scopus 로고
    • Flexible protocol for the Chemo- and regioselective building of pyrroles and pyrazoles by Reactions of Danishefsky's Dienes with 1,2-Diaza-1,3-butadienes
    • Attanasi, O.A.; Favi, G.; Filippone, P.; Giorgi, G.; Mantellini, F.; Moscatelli, G.; Spinelli, D. flexible protocol for the Chemo- and regioselective building of pyrroles and pyrazoles by Reactions of Danishefsky's Dienes with 1,2-Diaza-1,3-butadienes. Org. Lett., 2008, 10(10), 1983-1986.
    • (2008) Org. Lett , vol.10 , Issue.10 , pp. 1983-1986
    • Attanasi, O.A.1    Favi, G.2    Filippone, P.3    Giorgi, G.4    Mantellini, F.5    Moscatelli, G.6    Spinelli, D.7
  • 228
    • 45549094745 scopus 로고    scopus 로고
    • Base-Mediated reaction of hydrazones and nitroolefins with a reversed regioselectivity: A novel synthesis of 1,3,4-Trisubstituted Pyrazoles
    • Deng, X.; Mani, N.S. Base-Mediated reaction of hydrazones and nitroolefins with a reversed regioselectivity: A novel synthesis of 1,3,4-Trisubstituted Pyrazoles. Org. Lett., 2008, 10(6), 1307-1310.
    • (2008) Org. Lett , vol.10 , Issue.6 , pp. 1307-1310
    • Deng, X.1    Mani, N.S.2
  • 229
    • 45149147297 scopus 로고    scopus 로고
    • Silver(I)-Catalyzed Facile synthesis of pyrazoles From Propargyl N-Sulfonylhydrazones
    • Lee, Y.T.; Chung, Y.K. Silver(I)-Catalyzed Facile synthesis of pyrazoles From Propargyl N-Sulfonylhydrazones. J. Org. Chem., 2008, 73(12), 4698- 4701.
    • (2008) J. Org. Chem , vol.73 , Issue.12 , pp. 4698-4701
    • Lee, Y.T.1    Chung, Y.K.2
  • 230
    • 45149100137 scopus 로고    scopus 로고
    • Simple approach to some N-(5-Hydroxy- 1-phenyl-1H-pyrazol-4-yl)benzamides
    • Čuček, K.; Golobi A.; Verek, B. Simple approach to some N-(5-Hydroxy- 1-phenyl-1H-pyrazol-4-yl)benzamides. Heterocycles, 2007, 73(1), 555-566.
    • (2007) Heterocycles , vol.73 , Issue.1 , pp. 555-566
    • Čuček, K.1    Golobi, A.2    Verek, B.3
  • 231
    • 29744448555 scopus 로고    scopus 로고
    • Preparation and reactions of 3-phosphinyl-1-aza-1,3-butadienes. Synthesis of phosphorylated pyridine and pyrazole derivatives
    • Palacios, F.; Aparicio, D.; López, Y.; de los Santos, J.M.; Ezpeleta, J.M. Preparation and reactions of 3-phosphinyl-1-aza-1,3-butadienes. Synthesis of phosphorylated pyridine and pyrazole derivatives. Tetrahedron, 2006, 62, 1095-1101.
    • (2006) Tetrahedron , vol.62 , pp. 1095-1101
    • Palacios, F.1    Aparicio, D.2    López, Y.3    de los Santos, J.M.4    Ezpeleta, J.M.5
  • 232
    • 46149089401 scopus 로고    scopus 로고
    • A facile and convenient approach to the synthesis of 3,5-diaryl-1H-pyrazoles
    • Nikpour, F.; Beigvand, M. A facile and convenient approach to the synthesis of 3,5-diaryl-1H-pyrazoles. Monatsh. Chem., 2008, 139, 821-824.
    • (2008) Monatsh. Chem , vol.139 , pp. 821-824
    • Nikpour, F.1    Beigvand, M.2
  • 235
    • 45249111549 scopus 로고    scopus 로고
    • Facile and straightforward method leading to substituted 4-Amino-1-arylpyrazoles
    • Šimnek, P.; Svobodová, M.; Bertolasi, V.; Macháček, V. Facile and straightforward method leading to substituted 4-Amino-1-arylpyrazoles. Synthesis, 2008, (11), 1761-1766.
    • (2008) Synthesis , vol.11 , pp. 1761-1766
    • Šimnek, P.1    Svobodová, M.2    Bertolasi, V.3    Macháček, V.4
  • 236
    • 0037074195 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of new pyrazole- and tetrazole- related C-nucleosides with modified sugar moieties
    • Popsavin, M.; Torovi, L.; Spai, S.; Stankov, S.; Kapor, A.; Tomi, Z.; Popsavin, V. Synthesis and biological evaluation of new pyrazole- and tetrazole- related C-nucleosides with modified sugar moieties. Tetrahedron, 2002, 58, 569-580.
    • (2002) Tetrahedron , vol.58 , pp. 569-580
    • Popsavin, M.1    Torovi, L.2    Spai, S.3    Stankov, S.4    Kapor, A.5    Tomi, Z.6    Popsavin, V.7
  • 237
    • 57149131220 scopus 로고    scopus 로고
    • A novel synthesis of 1,3,5- trisubstituted pyrazoles through a spiro-pyrazoline intermediate via a tandem 1,3-dipolar cycloaddition/elimination
    • Dadiboyena, S.; Valente, E.J.; Hamme II, A.T. A novel synthesis of 1,3,5- trisubstituted pyrazoles through a spiro-pyrazoline intermediate via a tandem 1,3-dipolar cycloaddition/elimination. Tetrahedron Lett., 2009, 50, 291-294.
    • (2009) Tetrahedron Lett , vol.50 , pp. 291-294
    • Dadiboyena, S.1    Valente, E.J.2    Hamme II, A.T.3
  • 238
    • 34848859255 scopus 로고    scopus 로고
    • Synthesis of pentafluorosulfanylpyrazole and pentafluorosulfanyl-1,2,3- triazole and Their derivatives as Energetic materials by click chemistry
    • Ye, C.; Gard, G.L.; Winter, R.W.; Syvret, R.G.; Twamley, B.; Shreeve, J.M. Synthesis of pentafluorosulfanylpyrazole and pentafluorosulfanyl-1,2,3- triazole and Their derivatives as Energetic materials by click chemistry. Org. Lett., 2007, 9(19), 3841-3844.
    • (2007) Org. Lett , vol.9 , Issue.19 , pp. 3841-3844
    • Ye, C.1    Gard, G.L.2    Winter, R.W.3    Syvret, R.G.4    Twamley, B.5    Shreeve, J.M.6
  • 239
    • 0037533016 scopus 로고    scopus 로고
    • Novel one-pot method for the preparation of pyrazoles by 1,3-Dipolar cycloadditions of diazo compounds generated in situ
    • Aggarwal, V.K.; de Vicente, J.; Bonnert, R.V. A Novel one-pot method for the preparation of pyrazoles by 1,3-Dipolar cycloadditions of diazo compounds generated in situ. J. Org. Chem., 2003, 68, 5381-5383.
    • (2003) J. Org. Chem , vol.68 , pp. 5381-5383
    • Aggarwal, V.K.1    de Vicente, J.2    Bonnert, R.V.A.3
  • 240
    • 70149100867 scopus 로고    scopus 로고
    • New one-pot synthesis of pyrazole-5-carboxylates by 1,3-dipole cycloadditions of ethyl diazoacetate with-methylene carbonyl compounds
    • Gioiello, A.; Khamidullina, A.; Fulco, M.C.; Venturoni, F.; Zlotsky, S.; Pellicciari, R. New one-pot synthesis of pyrazole-5-carboxylates by 1,3-dipole cycloadditions of ethyl diazoacetate with-methylene carbonyl compounds. Tetrahedron Lett., 2009, 50(44), 5978-5980.
    • (2009) Tetrahedron Lett , vol.50 , Issue.44 , pp. 5978-5980
    • Gioiello, A.1    Khamidullina, A.2    Fulco, M.C.3    Venturoni, F.4    Zlotsky, S.5    Pellicciari, R.6
  • 241
    • 34248586827 scopus 로고    scopus 로고
    • A regioselective route to 5-substituted pyrazole- and pyrazoline-3-phosphonic acids and esters
    • Conti, P.; Pinto, A.; Tamborini, L.; Rizzo, V.; De Micheli, C. A regioselective route to 5-substituted pyrazole- and pyrazoline-3-phosphonic acids and esters. Tetrahedron, 2007, 63(25), 5554-5560.
    • (2007) Tetrahedron , vol.63 , Issue.25 , pp. 5554-5560
    • Conti, P.1    Pinto, A.2    Tamborini, L.3    Rizzo, V.4    de Micheli, C.5
  • 242
    • 0037429086 scopus 로고    scopus 로고
    • Nitrilimine cycloaddition to 4- (pyrazol-5-yl)carbonyl-2-azetidinone and 4-(pyrazol-4-yl)carbonyl-2-azetidinone
    • Del Buttero, P.; Moltenia, G.; Pilatib, T. Nitrilimine cycloaddition to 4- (pyrazol-5-yl)carbonyl-2-azetidinone and 4-(pyrazol-4-yl)carbonyl-2- azetidinone. Tetrahedron Lett., 2003, 44, 1425-1427.
    • (2003) Tetrahedron Lett , vol.44 , pp. 1425-1427
    • Del Buttero, P.1    Moltenia, G.2    Pilatib, T.3
  • 243
    • 74749088348 scopus 로고    scopus 로고
    • Synthesis of novel pyrazoles via [2+3]-dipolar cycloaddition using alkyne surrogates
    • Dadiboyena, S.; Valente, E.J.; Hamme II, A.T. Synthesis of novel pyrazoles via [2+3]-dipolar cycloaddition using alkyne surrogates. Tetrahedron Lett., 2010, 51(9), 1341-1343.
    • (2010) Tetrahedron Lett , vol.51 , Issue.9 , pp. 1341-1343
    • Dadiboyena, S.1    Valente, E.J.2    Hamme II, A.T.3
  • 244
    • 36448943266 scopus 로고    scopus 로고
    • An efficient synthesis of 2- Diazo-2-(trimethylsilyl)ethanols and their application to pyrazole synthesis
    • Hari, Y.; Tsuchida, S.; Sone, R.; Aoyama, T. An efficient synthesis of 2- Diazo-2-(trimethylsilyl)ethanols and their application to pyrazole synthesis. Synthesis, 2007, (21), 3371-3375.
    • (2007) Synthesis , Issue.21 , pp. 3371-3375
    • Hari, Y.1    Tsuchida, S.2    Sone, R.3    Aoyama, T.4
  • 245
    • 33947609921 scopus 로고    scopus 로고
    • Base-Mediated reaction of the Bestmann Ohira reagent with nitroalkenes for the Regioselective synthesis of phosphonylpyrazoles
    • Muruganantham, R.; Mobin, S.M.; Namboothiri, I.N.N. Base-Mediated reaction of the Bestmann Ohira reagent with nitroalkenes for the Regioselective synthesis of phosphonylpyrazoles. Org. Lett., 2007, 9(6), 1125-1128.
    • (2007) Org. Lett , vol.9 , Issue.6 , pp. 1125-1128
    • Muruganantham, R.1    Mobin, S.M.2    Namboothiri, I.N.N.3
  • 246
    • 33745725835 scopus 로고    scopus 로고
    • Novel synthesis of highly functionalized pyrazolines and pyrazoles by triphenylphosphine-mediated reaction of dialkyl azodicarboxylate with allenic esters
    • Nair, V.; Biju, A.T.; Mohanan, K.; Suresh, E. Novel synthesis of highly functionalized pyrazolines and pyrazoles by triphenylphosphine-mediated reaction of dialkyl azodicarboxylate with allenic esters. Org. Lett., 2006, 8(11), 2213-2216.
    • (2006) Org. Lett , vol.8 , Issue.11 , pp. 2213-2216
    • Nair, V.1    Biju, A.T.2    Mohanan, K.3    Suresh, E.4
  • 247
    • 53849083120 scopus 로고    scopus 로고
    • Allenylphosphonates-useful precursors of pyrazoles and 1,2,3-Triazoles
    • Chakravarty, M.; Kumar, N.N.B.; Sajna, K.V.; Swamy, K.C.K. Allenylphosphonates-useful precursors of pyrazoles and 1,2,3-Triazoles. Eur. J. Org. Chem., 2008, (26), 4500-4510.
    • (2008) Eur. J. Org. Chem , vol.26 , pp. 4500-4510
    • Chakravarty, M.1    Kumar, N.N.B.2    Sajna, K.V.3    Swamy, K.C.K.4
  • 248
    • 33751213878 scopus 로고    scopus 로고
    • Microwave-assisted synthesis of pyrazoles by 1,3-Dipolar cycloaddition of diazo compounds to acetylene derivatives
    • Zrinski, I.; Juribasic, M.; Eckert-Maksic, M. Microwave-assisted synthesis of pyrazoles by 1,3-Dipolar cycloaddition of diazo compounds to acetylene derivatives. Heterocycles, 2006, 68(9), 1961-1967.
    • (2006) Heterocycles , vol.68 , Issue.9 , pp. 1961-1967
    • Zrinski, I.1    Juribasic, M.2    Eckert-Maksic, M.3
  • 249
    • 63649120694 scopus 로고    scopus 로고
    • 1,3-Dipolar cycloaddition of diazoacetate compounds to terminal alkynes promoted by Zn(OTf)2: An efficient way to the preparation of pyrazoles
    • He, S.; Chen, L.; Niu, Y.-N.; Wu, L.-Y.; Liang, Y.-M. 1,3-Dipolar cycloaddition of diazoacetate compounds to terminal alkynes promoted by Zn(OTf)2: an efficient way to the preparation of pyrazoles. Tetrahedron Lett., 2009, 50(20), 2443-2445.
    • (2009) Tetrahedron Lett , vol.50 , Issue.20 , pp. 2443-2445
    • He, S.1    Chen, L.2    Niu, Y.-N.3    Wu, L.-Y.4    Liang, Y.-M.5
  • 250
    • 66149125218 scopus 로고    scopus 로고
    • One-pot synthesis of Narylpyrazoles from arylhalides
    • Gerstenberger, B.S.; Rauckhorst, M.R.; Starr, J.T. One-pot synthesis of Narylpyrazoles from arylhalides. Org. Lett., 2009, 11(10), 2097-2100.
    • (2009) Org. Lett , vol.11 , Issue.10 , pp. 2097-2100
    • Gerstenberger, B.S.1    Rauckhorst, M.R.2    Starr, J.T.3
  • 251
    • 77951554730 scopus 로고    scopus 로고
    • A sydnone cycloaddition route to pyrazole boronic esters
    • Browne, D.L.; Helm, M.D.; Plant, A.; Harrity, J.P.A. A sydnone cycloaddition route to pyrazole boronic esters. Angew. Chem., 2007, 119(45), 8810-8812;
    • (2007) Angew. Chem , vol.119 , Issue.45 , pp. 8810-8812
    • Browne, D.L.1    Helm, M.D.2    Plant, A.3    Harrity, J.P.A.4
  • 252
    • 36549038697 scopus 로고    scopus 로고
    • A sydnone cycloaddition route to pyrazole boronic esters
    • A sydnone cycloaddition route to pyrazole boronic esters. Angew. Chem. Int. Ed., 2007, 46, 8656-8658.
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 8656-8658
  • 253
    • 33645759529 scopus 로고    scopus 로고
    • Convenient and Efficient synthesis of pyrazole-Based DHODase inhibitors from 3- Aryl-4-cyanosydnone
    • Chang, E.-M.; Chen, T.-H.; Wong, F.F.; Chang, E.-C.; Yeh, M.-Y. Convenient and Efficient synthesis of pyrazole-Based DHODase inhibitors from 3- Aryl-4-cyanosydnone. Synlett, 2006, (6), 901-904.
    • (2006) Synlett , vol.6 , pp. 901-904
    • Chang, E.-M.1    Chen, T.-H.2    Wong, F.F.3    Chang, E.-C.4    Yeh, M.-Y.5
  • 254
    • 71749097873 scopus 로고    scopus 로고
    • Recent developments in the chemistry of sydnones
    • Browne, D.L.; Harrity, J.P.A. Recent developments in the chemistry of sydnones. Tetrahedron, 2010, 66(3), 553-568.
    • (2010) Tetrahedron , vol.66 , Issue.3 , pp. 553-568
    • Browne, D.L.1    Harrity, J.P.A.2
  • 255
    • 33745852809 scopus 로고    scopus 로고
    • Regioselectivity in 1,3-Dipolar Cycloaddition of 3-(4-Ethoxyphenyl)-4-cyanosydnone with propargylic esters
    • Chang, E.-M.; Wong, F.F.; Chen, T.-H.; Chiang, K.-C.; Yeh, M.-Y. Regioselectivity in 1,3-Dipolar Cycloaddition of 3-(4-Ethoxyphenyl)-4-cyanosydnone with propargylic esters. Heterocycles, 2006, 68(5), 1007-1015.
    • (2006) Heterocycles , vol.68 , Issue.5 , pp. 1007-1015
    • Chang, E.-M.1    Wong, F.F.2    Chen, T.-H.3    Chiang, K.-C.4    Yeh, M.-Y.5
  • 256
    • 58149305979 scopus 로고    scopus 로고
    • Cross coupling of Bromo sydnones: Development of a Flexible Route toward Functionalized pyrazoles
    • Browne, D.L.; Taylor, J.B.; Plant, A.; Harrity, J.P.A. Cross coupling of Bromo sydnones: development of a Flexible Route toward Functionalized pyrazoles. J. Org. Chem., 2009, 74, 396-400.
    • (2009) J. Org. Chem , vol.74 , pp. 396-400
    • Browne, D.L.1    Taylor, J.B.2    Plant, A.3    Harrity, J.P.A.4
  • 257
    • 66149124436 scopus 로고    scopus 로고
    • Solid-Phase synthesis of amino acid derived N-Unsubstituted pyrazoles via sydnones
    • Harju, K.; Vesterinen, J.; Yli-Kauhaluoma, J. Solid-Phase synthesis of amino acid derived N-Unsubstituted pyrazoles via sydnones. Org. Lett., 2009, 11(10), 2219-2221.
    • (2009) Org. Lett , vol.11 , Issue.10 , pp. 2219-2221
    • Harju, K.1    Vesterinen, J.2    Yli-Kauhaluoma, J.3
  • 258
    • 0034620920 scopus 로고    scopus 로고
    • Facile synthesis of pyrazoles and pyrroles via thermolysis of tetrazolo[1,5-b]pyridazines, tetrazolo[1,5-a]pyrimidines and tetrazolo[1,5-a]pyridines
    • Simoni, D.; Rondanin, R.; Furnò, G.; Aiello, E.; Invidiata, F.P. Facile synthesis of pyrazoles and pyrroles via thermolysis of tetrazolo[1,5-b]pyridazines, tetrazolo[1,5-a]pyrimidines and tetrazolo[1,5-a]pyridines. Tetrahedron Lett., 2000, 41(15), 2699-2703.
    • (2000) Tetrahedron Lett , vol.41 , Issue.15 , pp. 2699-2703
    • Simoni, D.1    Rondanin, R.2    Furnò, G.3    Aiello, E.4    Invidiata, F.P.5
  • 260
    • 44349113673 scopus 로고    scopus 로고
    • Three ways of reactions of 5-(3,5-dimethyl-1 H - pyrazol-1-yl)-2-phenyl-1,3-oxazole-4-carbonitrile and its analogs with nitrogen- containing bases
    • Three ways of reactions of 5-(3,5-dimethyl-1 H - pyrazol-1-yl)-2-phenyl-1,3-oxazole-4-carbonitrile and its analogs with nitrogen- containing bases. Russ. J. Gen. Chem., 2008, 78(4), 655.
    • (2008) Russ. J. Gen. Chem , vol.78 , Issue.4 , pp. 674
  • 261
    • 14844350074 scopus 로고    scopus 로고
    • Oxaziridine-mediated amination of primary amines: Scope and application to a one-pot pyrazole synthesis
    • Armstrong, A.; Jones, L.H.; Knight, J.D.; Kelsey, R.D. Oxaziridine-mediated amination of primary amines: Scope and application to a one-pot pyrazole synthesis. Org. Lett., 2005, 7(4), 713-716.
    • (2005) Org. Lett , vol.7 , Issue.4 , pp. 713-716
    • Armstrong, A.1    Jones, L.H.2    Knight, J.D.3    Kelsey, R.D.4
  • 263
    • 48849112035 scopus 로고    scopus 로고
    • Efficient and divergent synthesis of fully substituted 1H-Pyrazoles and isoxazoles from cyclopropyl oximes
    • Wang, K.; Xiang, D.; Liu, J.; Pan, W.; Dong, D. Efficient and divergent synthesis of fully substituted 1H-Pyrazoles and isoxazoles from cyclopropyl oximes. Org. Lett., 2008, 10(9), 1691-1694.
    • (2008) Org. Lett , vol.10 , Issue.9 , pp. 1691-1694
    • Wang, K.1    Xiang, D.2    Liu, J.3    Pan, W.4    Dong, D.5
  • 264
    • 0038765391 scopus 로고    scopus 로고
    • An Alternative Route for Carboni Lindsey Reaction: N,N Cycloaddition of an Alkene to s-Tetrazine
    • Zhou, X.; Kovalev (the late), E.G.; Klug, J.T.; Khodorkovsky, V. An Alternative Route for Carboni Lindsey Reaction: N,N Cycloaddition of an Alkene to s-Tetrazine. Org. Lett., 2001, 3(11), 1725-1727.
    • (2001) Org. Lett , vol.3 , Issue.11 , pp. 1725-1727
    • Zhou, X.1    Kovalev, E.G.2    Klug, J.T.3    Khodorkovsky, V.4
  • 265
    • 67650541096 scopus 로고    scopus 로고
    • The conversion of isothiazoles into pyrazoles using hydrazine
    • Ioannidou, H.A.; Koutentis, P.A. The conversion of isothiazoles into pyrazoles using hydrazine. Tetrahedron, 2009, 65(34), 7023-7037.
    • (2009) Tetrahedron , vol.65 , Issue.34 , pp. 7023-7037
    • Ioannidou, H.A.1    Koutentis, P.A.2
  • 266
    • 35348998945 scopus 로고    scopus 로고
    • Straightforward transformation of isoxazoles into pyrazoles: Renewed and improved
    • Sviridov, S.I.; Vasil'ev, A.A.; Shorshnev, S.V. Straightforward transformation of isoxazoles into pyrazoles: renewed and improved. Tetrahedron, 2007, 63(49), 12195-12201.
    • (2007) Tetrahedron , vol.63 , Issue.49 , pp. 12195-12201
    • Sviridov, S.I.1    Vasil'ev, A.A.2    Shorshnev, S.V.3
  • 268
    • 24644451095 scopus 로고    scopus 로고
    • 5-Phenyl-2- (pyrazol-4-yl)-1,3,4-thiadiazoles
    • 5-Phenyl-2- (pyrazol-4-yl)-1,3,4-thiadiazoles. Chem. Heterocycl. Comp. 2005, 41(5), 673-678.
    • (2005) Chem. Heterocycl. Comp , vol.41 , Issue.5 , pp. 673-678
  • 269
    • 33750623389 scopus 로고    scopus 로고
    • Domino Cu-catalyzed C-N coupling/ hydroamidation: A highly efficient synthesis of nitrogen heterocycles
    • Martín, R.; Rivero, M.R.; Buchwald, S.L. Domino Cu-catalyzed C-N coupling/ hydroamidation: a highly efficient synthesis of nitrogen heterocycles. Angew. Chem. Int. Ed., 2006, 45, 7079-7082.
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 7079-7082
    • Martín, R.1    Rivero, M.R.2    Buchwald, S.L.3
  • 270
    • 51149116300 scopus 로고    scopus 로고
    • A Regiospecific Approach to N-Alkylpyrazoles and the derived N-oxides using 5-endo-dig cyclisations of alkynyl nitrosamines
    • Hayes, S.J.; Knight, D.W.; ÓHalloran, M.; Pickering, S.R. A Regiospecific Approach to N-Alkylpyrazoles and the derived N-oxides using 5-endo-dig cyclisations of alkynyl nitrosamines. Synlett, 2008, (14), 2188-2190.
    • (2008) Synlett , vol.14 , pp. 2188-2190
    • Hayes, S.J.1    Knight, D.W.2    ÓHalloran, M.3    Pickering, S.R.4
  • 271
    • 0037882618 scopus 로고    scopus 로고
    • Oxidative Aromatization of 1,3,5-trisubstituted pyrazolines and hantzsch 1,4-dihydropyridines by Pd/C in acetic acid
    • Nakamichi, N.; Kawashita, Y.; Hayashi, M. Oxidative Aromatization of 1,3,5-trisubstituted pyrazolines and hantzsch 1,4-dihydropyridines by Pd/C in acetic acid. Org. Lett., 2002, 4(22), 3955-3957.
    • (2002) Org. Lett , vol.4 , Issue.22 , pp. 3955-3957
    • Nakamichi, N.1    Kawashita, Y.2    Hayashi, M.3
  • 272
    • 43849088792 scopus 로고    scopus 로고
    • Silica Sulfuric Acid-Activated Poly-1,3,-dichloro-5-methyl-5(4'-vinylphenyl)hydantoin (PDCVH) as an Effective reagent for oxidation of 1,3,5-trisubstituted 2-pyrazolines both under microwave irradiation and thermal condition
    • Azarifar, D.; Maleki, B.; Setayeshnazar, M. Silica Sulfuric Acid-Activated Poly-1,3,-dichloro-5-methyl-5(4'-vinylphenyl)hydantoin (PDCVH) as an Effective reagent for oxidation of 1,3,5-trisubstituted 2-pyrazolines both under microwave irradiation and thermal condition. Heterocycles, 2008, 75(3), 669-673.
    • (2008) Heterocycles , vol.75 , Issue.3 , pp. 669-673
    • Azarifar, D.1    Maleki, B.2    Setayeshnazar, M.3
  • 273
    • 33746013175 scopus 로고    scopus 로고
    • Microwave-promoted aromatization of 1,3,5- trisubstituted 4,5-Dihydro-1H-pyrazoles by calcium hypochlorite under Solvent- free Conditions
    • Azarifar, D.; Gharshasbi, A. Microwave-promoted aromatization of 1,3,5- trisubstituted 4,5-Dihydro-1H-pyrazoles by calcium hypochlorite under Solvent- free Conditions. Heterocycles, 2006, 68(6), 1209-1215.
    • (2006) Heterocycles , vol.68 , Issue.6 , pp. 1209-1215
    • Azarifar, D.1    Gharshasbi, A.2
  • 274
    • 26044462279 scopus 로고    scopus 로고
    • Microwave-assisted aromatization of 1,3,5- trisubstituted 2-pyrazolines by silica-supported N-bromosuccinimide as a useful reagent under solvent free 'dry' condition
    • Azarifar, D.; Maleki, B. microwave-assisted aromatization of 1,3,5- trisubstituted 2-pyrazolines by silica-supported N-bromosuccinimide as a useful reagent under solvent free 'dry' condition. Heterocycles, 2005, 65(4), 865-870.
    • (2005) Heterocycles , vol.65 , Issue.4 , pp. 865-870
    • Azarifar, D.1    Maleki, B.2
  • 275
    • 2542504592 scopus 로고    scopus 로고
    • Activated carbon-promoted oxidative aromatization of hantzsch 1,4-dihydropyridines and 1,3,5- trisubstituted pyrazolines using molecular oxygen
    • Nakamichi, N.; Kawashita, Y.; Hayashi, M. activated carbon-promoted oxidative aromatization of hantzsch 1,4-dihydropyridines and 1,3,5- trisubstituted pyrazolines using molecular oxygen. Synthesis, 2004, (7), 1015-1020.
    • (2004) Synthesis , vol.7 , pp. 1015-1020
    • Nakamichi, N.1    Kawashita, Y.2    Hayashi, M.3
  • 276
    • 0037711699 scopus 로고    scopus 로고
    • Zr(NO3)4: A versatile oxidizing agent for aromatization of hantzsch 1,4-dihydropyridines and 1,3,5-trisubstituted pyrazolines
    • Sabitha, G.; Kiran Kumar Reddy, G.S.; Srinivas Reddy, C.; Fatima, N.; Yadav, J.S. Zr(NO3)4: a versatile oxidizing agent for aromatization of hantzsch 1,4-dihydropyridines and 1,3,5-trisubstituted pyrazolines. Synthesis, 2003, (8), 1267-1271.
    • (2003) Synthesis , vol.8 , pp. 1267-1271
    • Sabitha, G.1    Kiran, K.R.G.S.2    Srinivas, R.C.3    Fatima, N.4    Yadav, J.S.5


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