메뉴 건너뛰기




Volumn 31, Issue 11, 2012, Pages 783-800

Synthesis and antimicrobial evaluation of novel pyrazolones and pyrazolone nucleosides

Author keywords

acyclic nucleosides; antimicrobial activity; N 2 Alkyl pyrazolones; Pyrazolinone; pyrazolono nucleosides

Indexed keywords

1 (4 HYDROXYBUTYL) 3 METHYL 4 (2 4 TOLYLHYDRAZONO) 1H PYRAZOL 5(4H) ONE; 1 (4 HYDROXYBUTYL) 3 METHYL 4 (2 PHENYLHYDRAZONO) 1H PYRAZOL 5(4H) ONE; 1 (4 HYDROXYBUTYL) 3 METHYL 4 [2 (4 NITROPHENYL)HYDRAZONO] 1H PYRAZOL 5(4H) ONE; 1 (BETA DEXTRO GLUCOPYRANOSYL) 3 METHYL 4(2 4 TOLYLHYDRAZONO) 1 H PYRAZOL 5(4H) ONE; 1 (BETA DEXTRO GLUCOPYRANOSYL) 4 [2 (4 METHOXY)PHENYLHYDRAZONO] 3 METHYL 1H PYRAZOL 5(4H) ONE; 1 [(2 HYDROXYETHOXY)METHYL] 3 METHYL 4 (2 4 TOLYLHYDRAZONO) 1H PYRAZOL 5(4H) ONE; 1 ALLYL 3 METHYL 4 (2 PHENYLHYDRAZONO) 1H PYRAZOL 5(4H) ONE; 1 ALLYL 3 METHYL 4 [2 (4 NITROPHENYL)HYDRAZONO] 1H PYRAZOL 5(4H) ONE; 1 ALLYL 4 [2 (4 METHOXYPHENYL)HYDRAZONO] 3 METHYL 1H PYRAZOL 5(4H) ONE; 3 METHYL 1 (BETA DEXTRO RIBOFURANOSYL) 4 (2 PHENYLHYDRAZONO) 1H PYRAZOL 5(4H) ONE; 3 METHYL 1 (PROP 2 YNYL) 4 (2 4 TOLYLHYDRAZONO) 1H PYRAZOL 5(4H) ONE; 3 METHYL 4 (2 4 TOLYLHYDRAZONO) 1H PYRAZOL 5(4H) ONE; 3 METHYL 4 (2 PHENYLHYDRAZONO) 1 (PROP 2 YNYL) 1H PYRAZOL 5(4H) ONE; 3 METHYL 4 (2 PHENYLHYDRAZONO) 1H PYRAZOL 5(4H) ONE; 3 METHYL 4 [2 (3 (TRIFLUOROMETHYL)PHENYLHYDRAZONO] 1H PYRAZOL 5(4H) ONE; 3 METHYL 4 [2 (4 NITROPHENYL)HYDRAZONO] 1H PYRAZOL 5(4H) ONE; 4 [2 (3 CHLOROPHENYL)HYDRAZONO] 3 METHYL 1 (PROP 2 YNYL) 1H PYRAZOL 5(4H) ONE; 4 [2 (3 CHLOROPHENYL)HYDRAZONO] 3 METHYL 1H PYRAZOL 5(4H) ONE; 4 [2 (4 BROMOPHENYL)HYDRAZONO] 1 (2 HYDROXYETHOXY)METHYL 3 METHYL 1H PYRAZOL 5(H) ONE; 4 [2 (4 BROMOPHENYL)HYDRAZONO] 3 METHYL 1H PYRAZOL 5(4H) ONE; 4 [2 (4 FLUOROPHENYL)HYDRAZONO] 1 (BETA DEXTRO GLUCOPYRANOSYL) 3 METHYL 1H PYRAZOL 5(4H) ONE; 4 [2 (4 FLUOROPHENYL)HYDRAZONO] 1 [(2 HYDROXYETHOXY)METHYL] 3 METHYL 1H PYRAZOL 5(4H) ONE; 4 [2 (4 FLUOROPHENYL)HYDRAZONO] 3 METHYL 1H PYRAZOL 5(4H) ONE; 4 [2 (4 METHOXYPHENYL)HYDRAZONO] 3 METHYL 1 (PROP 2 YNYL) 1H PYRAZOL 5(4H) ONE; 4 [2 (4 METHOXYPHENYL)HYDRAZONO] 3 METHYL 1H PYRAZOL 5(4H) ONE; AMPICILLIN; ANTIBIOTIC AGENT; NUCLEOSIDE DERIVATIVE; PYRAZOLONE DERIVATIVE; RIBAVIRIN; UNCLASSIFIED DRUG;

EID: 84869822932     PISSN: 15257770     EISSN: 15322335     Source Type: Journal    
DOI: 10.1080/15257770.2012.732250     Document Type: Article
Times cited : (19)

References (46)
  • 1
    • 84862231983 scopus 로고    scopus 로고
    • Novel RNA base pair with higher specificity using single selenium atom
    • Sun, H.; Sheng, J.; Hassan, A.E.A.; Jiang, S.; Gan, J.; Huang, Z. Novel RNA base pair with higher specificity using single selenium atom. Nucleic Acids Res. 2012, 40(11), 5171.
    • (2012) Nucleic Acids Res , vol.40 , Issue.11 , pp. 5171
    • Sun, H.1    Sheng, J.2    Hassan, A.E.A.3    Jiang, S.4    Gan, J.5    Huang, Z.6
  • 6
    • 0015523596 scopus 로고
    • Broadspectrum antiviral activity of Virazole. 1-β-D-ribofuranosyl-1, 2,4-triazole-3-carboxamide
    • Sidwell, R.W., Huffman, J.H., Khare, G.P., Allen, L.B., Withowski, J.T., Robins, R.K. Broadspectrum antiviral activity of Virazole. 1-β-D- ribofuranosyl-1,2,4-triazole-3-carboxamide. Science 1972, 177, 705-706.
    • (1972) Science , vol.177 , pp. 705-706
    • Sidwell, R.W.1    Huffman, J.H.2    Khare, G.P.3    Allen, L.B.4    Withowski, J.T.5    Robins, R.K.6
  • 8
    • 84857244174 scopus 로고    scopus 로고
    • Treatment of hepatitis C: Current standard and future concepts
    • Wedemeyer, H.; Hardtke, S., Cornberg, M. Treatment of hepatitis C: Current standard and future concepts. Chemotherapie J. 2012, 21(1), 1-7.
    • (2012) Chemotherapie J , vol.21 , Issue.1 , pp. 1-7
    • Wedemeyer, H.1    Hardtke, S.2    Cornberg, M.3
  • 11
    • 0016803201 scopus 로고
    • Bredinin. II. Molecular structure of bredinin
    • Yoshioka, H.; Nakatsu, K.; Mizuno, K. Bredinin. II. Molecular structure of bredinin. Tetrahedron Lett. 1975, 46, 4031-4034.
    • (1975) Tetrahedron Lett , vol.46 , pp. 4031-4034
    • Yoshioka, H.1    Nakatsu, K.2    Mizuno, K.3
  • 13
    • 0026613776 scopus 로고
    • Locoregional immunosuppression of organ transplants
    • Gruber, S.A. Locoregional immunosuppression of organ transplants. Immunol. Rev. 1992, 129, 5-30.
    • (1992) Immunol. Rev , vol.129 , pp. 5-30
    • Gruber, S.A.1
  • 14
    • 0025821616 scopus 로고
    • Guanine ribonucleotide depletion inhibits T-cell activation. Mechanism of action of the immunosuppressive drug mizoribine
    • Truka, L.; Dayton, J.; Sinclair, G.; Thompson, C.B.; Mitchell, B.S. Guanine ribonucleotide depletion inhibits T-cell activation. Mechanism of action of the immunosuppressive drug mizoribine. J. Clin. Invest. 1991, 87(3), 940-948.
    • (1991) J. Clin. Invest , vol.87 , Issue.3 , pp. 940-948
    • Truka, L.1    Dayton, J.2    Sinclair, G.3    Thompson, C.B.4    Mitchell, B.S.5
  • 16
    • 0029982866 scopus 로고    scopus 로고
    • IMP dehydrogenase as a target of antitumor and antiviral chemotherapy
    • Franchetti, P.; Cappellacci, L. Grifantini, M. IMP dehydrogenase as a target of antitumor and antiviral chemotherapy. Farmaco 1996, 51(7), 457-469. (Pubitemid 26253798)
    • (1996) Farmaco , vol.51 , Issue.7 , pp. 457-469
    • Franchetti, P.1    Cappellacci, L.2    Grifantini, M.3
  • 17
    • 14344254281 scopus 로고    scopus 로고
    • Synthesis and structural characterization of some Schiff bases derived from 4-[{(aryl)imino}ethyl]-3-methyl-1-(4′-methylphenyl)-2-pyrazolin-5-one and spectroscopic studies of their Cu(II) complexes
    • DOI 10.1016/j.poly.2004.07.025
    • Jedeja, R.N.J.; Shah, R.; Suresh, E.; Paul, P. Synthesis and structural characterization of some Schiff bases derived from 4-[{(aryl)imino}ethyl]-3- methyl-1-(4'-methylphenyl)-2-pyrazolin-5-one and spectroscopic studies of their Cu(II) complexes. Polyhedron 2004, 23, 2465-2474. (Pubitemid 40292102)
    • (2004) Polyhedron , vol.23 , Issue.16 , pp. 2465-2474
    • Jadeja, R.N.1    Shah, J.R.2    Suresh, E.3    Paul, P.4
  • 18
    • 0342368828 scopus 로고    scopus 로고
    • Synthesis and preliminary evaluation of new 5-pyrazolinone derivatives as analgesic agents
    • DOI 10.1016/S0223-5234(00)00117-3
    • G̈ursoy, A.; Demirayak, M.S.; Capan, G.; Erol, K. Synthesis and preliminary evaluation of new 5-pyrazolinone derivatives as analgesic agents. Eur. J. Med. Chem. 2000, 35, 359-364. (Pubitemid 30187068)
    • (2000) European Journal of Medicinal Chemistry , vol.35 , Issue.3 , pp. 359-364
    • Gursoy, A.1    Demirayak, S.2    Capan, G.3    Erol, K.4    Vural, K.5
  • 19
    • 0032102385 scopus 로고    scopus 로고
    • Nonsteroidal antiinflammatory agents. Part 1: Antiinflammatory, analgesic and antipyretic activity of some new 1-(pyrimidin-2-yl)-3-pyrazolin-5-ones and 2-(pyrimidin-2-yl)-1, 2, 4,5,6,7-hexahydro-3H-indazol-3-ones
    • Badaway, E.A.M.; EL-Ashmawy, I.M. Nonsteroidal antiinflammatory agents. Part 1: Antiinflammatory, analgesic and antipyretic activity of some new 1-(pyrimidin-2-yl)-3-pyrazolin-5-ones and 2-(pyrimidin-2-yl)-1,2,4,5,6,7- hexahydro-3H-indazol-3-ones. Eur. J. Med. Chem. 1998, 33, 349-361.
    • (1998) Eur. J. Med. Chem , vol.33 , pp. 349-361
    • Badaway, E.A.M.1    El-Ashmawy, I.M.2
  • 21
    • 68949174082 scopus 로고    scopus 로고
    • A facile synthesis, structure, and antimicrobial evaluation of novel 4-Arylhydrazono-5-trifluoromethyl-2,4-dihydropyrazol-3-ones, their N-AndN,O-bis-β-D-glucosides
    • Nasser, S.A.M.K. A facile synthesis, structure, and antimicrobial evaluation of novel 4-Arylhydrazono-5-trifluoromethyl-2,4-dihydropyrazol-3-ones, their N-AndN,O-bis-β-D-glucosides. Carbohyd. Res. 2009, 344, 1654-1659.
    • (2009) Carbohyd. Res , vol.344 , pp. 1654-1659
    • Nasser, S.A.M.K.1
  • 22
    • 0035703804 scopus 로고    scopus 로고
    • Synthesis and potential antimicrobial activity of some new compounds containing the pyrazol-3-one moiety
    • Al-Haiza, M.A.; El-Assiery, S.A.; Sayed, G.H. Synthesis and potential antimicrobial activity of some new compounds containing the pyrazol-3-one moiety. Acta Pharm. 2001, 51, 251-261. (Pubitemid 34111856)
    • (2001) Acta Pharmaceutica , vol.51 , Issue.4 , pp. 251-261
    • Al-Haiza, M.A.1    El-Assiery, S.A.2    Sayed, G.H.3
  • 23
    • 33747095922 scopus 로고    scopus 로고
    • A pyrimidine-pyrazolone nucleoside chimera with potent in vitro anti-orthopoxvirus activity
    • DOI 10.1016/j.bmcl.2006.03.043, PII S0960894X06003362
    • Fan, X.; Zahng, X.; Zhou, L.K.; Keith, A.; Kern, E.R.; Torrence, P.F. A pyrimidine-pyrazolone nucleoside chimera with potent in vitro anti-orthopoxvirus activity. Bioorg. Med. Chem. Lett. 2006, 16, 3224-3228. (Pubitemid 44287967)
    • (2006) Bioorganic and Medicinal Chemistry Letters , vol.16 , Issue.12 , pp. 3224-3228
    • Fan, X.1    Zhang, X.2    Zhou, L.3    Keith, K.A.4    Kern, E.R.5    Torrence, P.F.6
  • 24
    • 17144421736 scopus 로고    scopus 로고
    • Preparation of pyrazolone derivatives as inhibitors of GSK-3, Aurora-2 and CDK-2
    • WO 2002-US24726
    • Green, J.; Arnost, Michael, J.; Pierce, A. Preparation of pyrazolone derivatives as inhibitors of GSK-3, Aurora-2 and CDK-2. PCT Int. Appl., WO 2002-US24726, 2003, pp. 143.
    • (2003) PCT Int. Appl. , pp. 143
    • Green, J.1    Arnost Michael, J.2    Pierce, A.3
  • 25
    • 76649095270 scopus 로고    scopus 로고
    • 3-Aryl-4-(arylhydrazono)-1H-pyrazol-5-ones: Highly ligand efficient and potent inhibitors of GSK3β
    • Arnost, M.; Pierce, A.; Ter Haar, E.; Lauffer, D.; Madden, J.; Tanner, K.; Green, J. 3-Aryl-4-(arylhydrazono)-1H-pyrazol-5-ones: Highly ligand efficient and potent inhibitors of GSK3β. Bioorg. Med. Chem. Lett. 2010, 20, 1661-1664.
    • (2010) Bioorg. Med. Chem. Lett , vol.20 , pp. 1661-1664
    • Arnost, M.1    Pierce, A.2    Ter Haar, E.3    Lauffer, D.4    Madden, J.5    Tanner, K.6    Green, J.7
  • 27
    • 84855802696 scopus 로고    scopus 로고
    • Synthesis and evaluation of the substrate activity of C-6 substituted purine ribosides with E. coli purine nucleoside phosphorylase: Palladium mediated cross-coupling of organo-zinc halides with 6-chloropurine nucleosides
    • Hassan, A.E.A.; Abou-Elkhair, R.A.I.; Allan, P.W.; Parker, W.B.; Waud, W.R.; Secrist III, J.A. Synthesis and evaluation of the substrate activity of C-6 substituted purine ribosides with E. coli purine nucleoside phosphorylase: Palladium mediated cross-coupling of organo-zinc halides with 6-chloropurine nucleosides. Eur. J. Med. Chem. 2012, 47, 167.
    • (2012) Eur. J. Med. Chem , vol.47 , pp. 167
    • Hassan, A.E.A.1    Abou-Elkhair, R.A.I.2    Allan, P.W.3    Parker, W.B.4    Waud, W.R.5    Secrist Iii., J.A.6
  • 29
    • 84891957464 scopus 로고    scopus 로고
    • 2-(2,3-,5-Tri-O-Acetyl-β-D-ribofuranosyl)-4-(p-tolylazo) -5-trifluoromethyl-2,4-dihydropyrazol-3-one
    • Haikal, A.; Zohdi, H.F.; Badi, Z. 2-(2,3-,5-Tri-O-Acetyl-β-D- ribofuranosyl)-4-(p-tolylazo)-5-trifluoromethyl-2,4-dihydropyrazol-3-one. Molbank 2003, M306.
    • (2003) Molbank
    • Haikal, A.1    Zohdi, H.F.2    Badi, Z.3
  • 30
    • 84891957464 scopus 로고    scopus 로고
    • 2-(β-D-Ribofuranosyl)-4-(p-tolylazo)-5-trifluoromethyl-2, 4-dihydropyrazol-3-one
    • Haikal, A.; Zohdi, H.F.; Badi, Z. 2-(β-D-Ribofuranosyl)-4-(p- tolylazo)-5-trifluoromethyl-2,4-dihydropyrazol-3-one. Molbank 2003, M307.
    • (2003) Molbank
    • Haikal, A.1    Zohdi, H.F.2    Badi, Z.3
  • 32
    • 45149110706 scopus 로고    scopus 로고
    • Three-component combinatorial synthesis of novel dihydropyrano[2,3-c] pyrazoles
    • Lehmann, F.; Holm, M.; Laufer, S. Three-Component Combinatorial Synthesis of Novel Dihydropyrano[2,3-c]pyrazoles. J. Comb. Chem. 2008, 10(3), 364-367.
    • (2008) J. Comb. Chem , vol.10 , Issue.3 , pp. 364-367
    • Lehmann, F.1    Holm, M.2    Laufer, S.3
  • 33
    • 84891948721 scopus 로고    scopus 로고
    • Study on synthesis of 3-methyl-5-pyrazolone
    • Liu, F.; Yu, S.; Xin, Z.; Ge, X. Study on synthesis of 3-methyl-5-pyrazolone. Huaxue Shijie 2003, 44(8), 426-427.
    • (2003) Huaxue Shijie , vol.44 , Issue.8 , pp. 426-427
    • Liu, F.1    Yu, S.2    Xin, Z.3    Ge, X.4
  • 34
    • 46249087876 scopus 로고    scopus 로고
    • Synthesis and structure elucidation of hydrazones derived from N-2,4-dimethylphenyl)-3-oxobutanamide
    • Murat, C.H.; Sevim, R.; Guniz, S.K.; Bedia, K.K. Synthesis and structure elucidation of hydrazones derived from N-(2,4-dimethylphenyl)-3-oxobutanamide. Arkivoc 2008, (xii), 188-194.
    • (2008) Arkivoc , vol.12 , pp. 188-194
    • Murat, C.H.1    Sevim, R.2    Guniz, S.K.3    Bedia, K.K.4
  • 35
    • 3342959859 scopus 로고    scopus 로고
    • Reactions with hydrazonyl halides. 31. Synthesis of some new pyrrolidinoo[3,4-c]pyrazolines, pyrazoles, and pyrazolo[3,4-d]pyridazine
    • Abdou, O.A.;Hussein, F.Z.; Mohamed, M.; Nagla, A.A. Reactions with hydrazonyl halides. 31. Synthesis of some new pyrrolidinoo[3,4-c]pyrazolines, pyrazoles, and pyrazolo[3,4-d]pyridazine. Molecules 2000, 5, 967-973.
    • (2000) Molecules , vol.5 , pp. 967-973
    • Abdou, O.A.1    Hussein, F.Z.2    Mohamed, M.3    Nagla, A.A.4
  • 36
    • 0008586238 scopus 로고
    • Tautomerism of heteroaromatic compounds with five-membered rings. IV. 1-Substituted pyrazolin-5-ones
    • Katritzky, A.R.; Maine, F.W. Tautomerism of heteroaromatic compounds with five-membered rings. IV. 1-Substituted pyrazolin-5-ones. Tetrahedron 1964, 20(2), 299-314.
    • (1964) Tetrahedron , vol.20 , Issue.2 , pp. 299-314
    • Katritzky, A.R.1    Maine, F.W.2
  • 37
    • 0033366366 scopus 로고    scopus 로고
    • Synthesis of some hetarylazopyrazolone dyes and solvent effects on their absorption spectra
    • Ertan, N. Synthesis of some hetarylazopyrazolone dyes and solvent effects on their absorption spectra. Dyes Pigments 2000, 44, 41-48.
    • (2000) Dyes Pigments , vol.44 , pp. 41-48
    • Ertan, N.1
  • 38
    • 33947334806 scopus 로고
    • The structure of 2-pyrazolin-5-one dyes
    • Yasuda, H.; Midorikawa, H. The structure of 2-pyrazolin-5-one dyes. J. Org. Chem. 1966, 3, 1722-1725.
    • (1966) J. Org. Chem , vol.3 , pp. 1722-1725
    • Yasuda, H.1    Midorikawa, H.2
  • 39
    • 0036853301 scopus 로고    scopus 로고
    • Hetarylazo disperse dyes derived from 3-methyl-1- (3′,5′- dipiperidino-s-triazinyl)-5-pyrazolone as coupling component
    • DOI 10.1016/S0143-7208(02)00102-X, PII S014372080200102X
    • Karci, F.; Ertan, N. Hetarylazo disperse dyes derived from 3-methyl-1-(3',5'-dipiperidino-s-triazinyl)-5-pyrazolone as coupling component. Dyes Pigments 2002, 55(2-3), 99-108. (Pubitemid 35374863)
    • (2002) Dyes and Pigments , vol.55 , Issue.2-3 , pp. 99-108
    • Karci, F.1    Ertan, N.2
  • 40
    • 78149265962 scopus 로고    scopus 로고
    • Magnesium coordination-directed N-selective stereospecific alkylation of 2-pyridones, carbamates, and amides using α-halocarboxylic acids
    • Fang, Y.Q.; Bio, M.M.; Hansen, K.B.; Potter, M.S.; Clausen, A. Magnesium coordination-directed N-selective stereospecific alkylation of 2-pyridones, carbamates, and amides using α-halocarboxylic acids. J. Amer. Chem. Soc. 2010, 132, 15525-15527.
    • (2010) J. Amer. Chem. Soc , vol.132 , pp. 15525-15527
    • Fang, Y.Q.1    Bio, M.M.2    Hansen, K.B.3    Potter, M.S.4    Clausen, A.5
  • 41
    • 77953200029 scopus 로고    scopus 로고
    • Microwave-Assisted click chemistry: Synthesis of mono and bis-1, 2,3-triazole acyclonucleoside analogues of Acyclovir via copper(I)-catalyzed cycloaddition
    • Krim, J.; Sillahi, B.; Taourirte, M.; Rakib, E.M.; Engels, J.W. Microwave-Assisted click chemistry: Synthesis of mono and bis-1,2,3-triazole acyclonucleoside analogues of Acyclovir via copper(I)-catalyzed cycloaddition. Arkivoc 2009, (xiii) 142-152.
    • (2009) Arkivoc , Issue.13 , pp. 142-152
    • Krim, J.1    Sillahi, B.2    Taourirte, M.3    Rakib, E.M.4    Engels, J.W.5
  • 42
    • 0019975382 scopus 로고
    • Nucleic acid related compounds. 37. Convenient and high-yield syntheses of N-[(2-hydroxyethoxy)methyl] heterocycles as 'acyclic nucleoside' analogues
    • DOI 10.1139/v82-081
    • Robins, M.J.; Hatfield, P.W.Nucleic acid related compounds. 37. Convenient and high-yield syntheses of N-[(2-hydroxyethoxy)methyl]heterocycles as "acyclic nucleoside" analogs. Can. J. Chem. 1982, 60, 547-553. (Pubitemid 12093636)
    • (1982) Canadian Journal of Chemistry , vol.60 , Issue.5 , pp. 547-553
    • Robins, M.J.1    Hatfield, P.W.2
  • 44
    • 79958824392 scopus 로고    scopus 로고
    • ZnCl2-catalysed synthesis of novel 4-Arylazo-3-methyl-1-(H/phenyl)- 1Hpyrazol-5(4H)-ones
    • Thakre, W.; Meshram, J. ZnCl2-catalysed synthesis of novel 4-Arylazo-3-methyl-1-(H/phenyl)-1Hpyrazol-5(4H)-ones. Indian. J. Hetrocycl. Chem. 2009, 19, 185-186.
    • (2009) Indian. J. Hetrocycl. Chem , vol.19 , pp. 185-186
    • Thakre, W.1    Meshram, J.2
  • 45
    • 13444281914 scopus 로고    scopus 로고
    • Metal salt-catalyzed diazocoupling of 3-substituted-1H-pyrazol-2-in-5- ones in aqueous medium
    • DOI 10.1016/j.dyepig.2004.10.005, PII S0143720804002608
    • Khalil, A.K.; Hassan, M.A.; Mohamed, M.M.; El-Sayed, A.M. Metal salt-catalyzed diazo coupling of 3-substituted-1H-pyrazol-2-in-5-ones in aqueous medium. Dyes Pigments 2005, 66, 241-245. (Pubitemid 40205442)
    • (2005) Dyes and Pigments , vol.66 , Issue.3 , pp. 241-245
    • Khalil, A.Kh.1    Hassan, M.A.2    Mohamed, M.M.3    El-Sayed, A.M.4
  • 46
    • 34547896637 scopus 로고    scopus 로고
    • Synthesis of some biologically active 3-methyl-4-(substituted phenylhydrazono)-2-pyrazolin-5-ones and 2-isoxazolin-5-ones
    • Rajput, A.; Rajput, P.S. Synthesis of some biologically active 3-methyl-4-(substituted phenylhydrazono)-2-pyrazolin-5-ones and 2-isoxazolin-5-ones. Asian J. Chem. 2007, 19(6), 4479-4482.
    • (2007) Asian J. Chem , vol.19 , Issue.6 , pp. 4479-4482
    • Rajput, A.1    Rajput, P.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.