메뉴 건너뛰기




Volumn 58, Issue 6, 2003, Pages 431-437

Synthesis, antibacterial and antifungal activities of electron-rich olefins derived benzimidazole compounds

Author keywords

Antibacterial activities; Antifungal activities; Benzimidazole derivatives; Electron rich olefins; In vitro studies

Indexed keywords

ALKENE DERIVATIVE; BENZIMIDAZOLE DERIVATIVE; BIS[1,3 BIS(2 PHENYLETHYL)BENZIMIDAZOLIDIN 2 YLIDENE]; REAGENT; UNCLASSIFIED DRUG;

EID: 0038630972     PISSN: 0014827X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0014-827X(03)00068-5     Document Type: Article
Times cited : (109)

References (27)
  • 1
    • 0042771951 scopus 로고
    • The coordination chemistry of electron-rich alkenes (enetetramines)
    • Lappert M.F. The coordination chemistry of electron-rich alkenes (enetetramines). J. Organomet. Chem. 358:1988;185-214.
    • (1988) J. Organomet. Chem. , vol.358 , pp. 185-214
    • Lappert, M.F.1
  • 2
    • 33748216594 scopus 로고
    • Structures of sterically overcrowded and charge-perturbed molecules. 12. Tetrakis(dimethylamino) ethene an extremely electron-rich molecule with unusual structure both in the crystal and in the gas-phase
    • Bock H., Borrmann H., Havlas Z., Oberhammer H., Ruppert K., Simon A. Structures of sterically overcrowded and charge-perturbed molecules. 12. tetrakis(dimethylamino) ethene an extremely electron-rich molecule with unusual structure both in the crystal and in the gas-phase. Angew. Chem., Int. Ed. Engl. 30:1991;1678-1681.
    • (1991) Angew. Chem., Int. Ed. Engl. , vol.30 , pp. 1678-1681
    • Bock, H.1    Borrmann, H.2    Havlas, Z.3    Oberhammer, H.4    Ruppert, K.5    Simon, A.6
  • 3
    • 37049138531 scopus 로고
    • Photoelectron spectra of electron-rich olefins and an isostructural boron compound olefins of exceptionally low first ionisation potential
    • B. Çetinkaya, G.H. King, S.S. Krishnamuthy, M.F. Lappert, J.B. Pedley, Photoelectron spectra of electron-rich olefins and an isostructural boron compound olefins of exceptionally low first ionisation potential, J. Chem. Soc., Chem. Commun. (1971) 1370-1.
    • (1971) J. Chem. Soc., Chem. Commun. , pp. 1370-1371
    • Çetinkaya, B.1    King, G.H.2    Krishnamuthy, S.S.3    Lappert, M.F.4    Pedley, J.B.5
  • 5
    • 0037533722 scopus 로고    scopus 로고
    • New (carbene) ruthenium-arene complexes: Preparation and uses in catalytic synthesis of furans
    • Küçükbay H., Çetinkaya B., Guesmi S., Dixneuf P.H. New (carbene) ruthenium-arene complexes: preparation and uses in catalytic synthesis of furans. Organometallics. 15:1996;2434-2439.
    • (1996) Organometallics , vol.15 , pp. 2434-2439
    • Küçükbay, H.1    Çetinkaya, B.2    Guesmi, S.3    Dixneuf, P.H.4
  • 6
    • 37049101338 scopus 로고
    • A new class of benzoin condensation catalyst, the bi-(1,3-dialkylimidazolidin-2-ylidenes)
    • M.F. Lappert, R.K. Maskell, A new class of benzoin condensation catalyst, the bi-(1,3-dialkylimidazolidin-2-ylidenes), J. Chem. Soc., Chem. Commun. (1982) 580-1.
    • (1982) J. Chem. Soc., Chem. Commun. , pp. 580-581
    • Lappert, M.F.1    Maskell, R.K.2
  • 7
    • 1842264898 scopus 로고
    • Effective acyloin condensations catalyzed by electron-rich olefins
    • Çetinkaya E., Küçükbay H. Effective acyloin condensations catalyzed by electron-rich olefins. Turk. J. Chem. 19:1995;24-30.
    • (1995) Turk. J. Chem. , vol.19 , pp. 24-30
    • Çetinkaya, E.1    Küçükbay, H.2
  • 8
    • 84980899326 scopus 로고
    • Ein nucleophiles carben
    • Wanzlick H.W., Schikora E. Ein nucleophiles carben. Chem. Ber. 94:1961;2389-2393.
    • (1961) Chem. Ber. , vol.94 , pp. 2389-2393
    • Wanzlick, H.W.1    Schikora, E.2
  • 9
    • 84981939406 scopus 로고
    • Reactions of electron-rich olefins with proton-active compounds
    • Hocker J., Merten R. Reactions of electron-rich olefins with proton-active compounds. Angew. Chem., Int. Ed. Engl. 11:1972;964-973.
    • (1972) Angew. Chem., Int. Ed. Engl. , vol.11 , pp. 964-973
    • Hocker, J.1    Merten, R.2
  • 10
  • 11
    • 84981371931 scopus 로고
    • Reaktionen von ethylentetraminen mit sulfonamiden und phosphororganischen verbindungen
    • J. Hocker, R. Merten, Reaktionen von ethylentetraminen mit sulfonamiden und phosphororganischen verbindungen, Leibigs Ann. Chem. 719 (1978) 16-28.
    • (1978) Leibigs Ann. Chem. , vol.719 , pp. 16-28
    • Hocker, J.1    Merten, R.2
  • 13
    • 0038813171 scopus 로고
    • Radical nature of [1,3]sigmatropic rearrangements of electron-rich olefins
    • Baldwin J.E., Branz S.E., Walker J.A. Radical nature of [1,3]sigmatropic rearrangements of electron-rich olefins. J. Org. Chem. 42:1977;4142-4144.
    • (1977) J. Org. Chem. , vol.42 , pp. 4142-4144
    • Baldwin, J.E.1    Branz, S.E.2    Walker, J.A.3
  • 15
    • 33748638041 scopus 로고    scopus 로고
    • Synthesis and structures of 1,3,1′,3′-tetrabenzyl-2,2′-biimidazolidin ylidenes (electron-rich alkenes), their aminal intermediates and their degradation products
    • Çetinkaya B., Çetinkaya E., Chamizo J.A., Hitchcock P.B., Jasim H.A., Küçükbay H., Lappert M.F. Synthesis and structures of 1,3,1′,3′-tetrabenzyl-2,2′-biimidazolidin ylidenes (electron-rich alkenes), their aminal intermediates and their degradation products. J. Chem. Soc., Perkin Trans. 1:1998;2047-2054.
    • (1998) J. Chem. Soc., Perkin Trans. , vol.1 , pp. 2047-2054
    • Çetinkaya, B.1    Çetinkaya, E.2    Chamizo, J.A.3    Hitchcock, P.B.4    Jasim, H.A.5    Küçükbay, H.6    Lappert, M.F.7
  • 16
    • 0346609918 scopus 로고    scopus 로고
    • A zwitterionic carbene-stannylene adduct via cleavage of a dibenzotetraazafulvalene by a stannylene
    • Hahn F.E., Wittenbecher L., Kühn M., Lügger T., Fröhlich R. A zwitterionic carbene-stannylene adduct via cleavage of a dibenzotetraazafulvalene by a stannylene. J. Organomet. Chem. 617-618:2001;629-634.
    • (2001) J. Organomet. Chem. , vol.617-618 , pp. 629-634
    • Hahn, F.E.1    Wittenbecher, L.2    Kühn, M.3    Lügger, T.4    Fröhlich, R.5
  • 18
    • 0026784671 scopus 로고
    • Synthesis of same hydroxamic acid derivatives of benzimidazole and their antibacterial and antifungal activities
    • Günes H.S., Cosar G. Synthesis of same hydroxamic acid derivatives of benzimidazole and their antibacterial and antifungal activities. Arzneim.-Forsch./Drug Res. 42:1992;1045-1048.
    • (1992) Arzneim.-Forsch./Drug Res. , vol.42 , pp. 1045-1048
    • Günes, H.S.1    Cosar, G.2
  • 19
    • 0008625468 scopus 로고    scopus 로고
    • Syntesis of some benzimidazole derivatives and their antibacterial and antifungal activities
    • Küçükbay H., Durmaz R., Güven M., Günal S. Syntesis of some benzimidazole derivatives and their antibacterial and antifungal activities. Arzneim.-Forsch./Drug Res. 51:2001;420-424.
    • (2001) Arzneim.-Forsch./Drug Res. , vol.51 , pp. 420-424
    • Küçükbay, H.1    Durmaz, R.2    Güven, M.3    Günal, S.4
  • 20
    • 0029565762 scopus 로고
    • Synthesis and antimicrobial activity of substituted benzimidazole, benzothiazole and imidazole derivatives
    • Küçükbay H., Çetinkaya E., Durmaz R. Synthesis and antimicrobial activity of substituted benzimidazole, benzothiazole and imidazole derivatives. Arzneim.-Forsch./Drug Res. 45:1995;1331-1334.
    • (1995) Arzneim.-Forsch./Drug Res. , vol.45 , pp. 1331-1334
    • Küçükbay, H.1    Çetinkaya, E.2    Durmaz, R.3
  • 21
    • 0030972257 scopus 로고
    • Antifungal activity of organic and organometallic derivatives of benzimidazole and benzothiazole
    • Küçükbay H., Durmaz B. Antifungal activity of organic and organometallic derivatives of benzimidazole and benzothiazole. Arzneim.-Forsch./Drug Res. 47:1995;667-670.
    • (1995) Arzneim.-Forsch./Drug Res. , vol.47 , pp. 667-670
    • Küçükbay, H.1    Durmaz, B.2
  • 24
    • 0344628870 scopus 로고    scopus 로고
    • Investigation of serum minimal inhibitory concentrations of some benzimidazole, imidazole and benzothiazole derivatives and their effects on liver and renal functions
    • Durmaz R., Köroglu M., Küçükbay H., Temel I., Özer M.K., Refiq M., Çetinkaya E., Çetinkaya B., Yologlu S. Investigation of serum minimal inhibitory concentrations of some benzimidazole, imidazole and benzothiazole derivatives and their effects on liver and renal functions. Arzneim.-Forsch./Drug Res. 48:1998;1179-1184.
    • (1998) Arzneim.-Forsch./Drug Res. , vol.48 , pp. 1179-1184
    • Durmaz, R.1    Köroglu, M.2    Küçükbay, H.3    Temel, I.4    Özer, M.K.5    Refiq, M.6    Çetinkaya, E.7    Çetinkaya, B.8    Yologlu, S.9
  • 27
    • 0035619984 scopus 로고    scopus 로고
    • Selenium speciation in Karakaya dam lake's water (TR-Turkey)
    • Küçükbay F.Z., Demir M. Selenium speciation in Karakaya dam lake's water (TR-Turkey). Turk. J. Chem. 25:2001;341-347.
    • (2001) Turk. J. Chem. , vol.25 , pp. 341-347
    • Küçükbay, F.Z.1    Demir, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.