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Volumn 24, Issue 11, 2013, Pages 993-996

An expedient one-pot synthesis of highly substituted imidazoles using supported ionic liquid-like phase (SILLP) as a green and efficient catalyst and evaluation of their anti-microbial activity

Author keywords

Anti microbial activities; Imidazole; Ionic liquid; Phenanthroimidazole; SILLP; Three component reaction

Indexed keywords


EID: 84886096236     PISSN: 10018417     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cclet.2013.06.005     Document Type: Article
Times cited : (35)

References (32)
  • 1
    • 0016259815 scopus 로고
    • Preparation and antiinflammatory activity of some nonacidic trisubstituted imidazoles
    • J.G. Lombardino, and E.H. Wiseman Preparation and antiinflammatory activity of some nonacidic trisubstituted imidazoles J. Med. Chem. 17 1974 1182 1188
    • (1974) J. Med. Chem. , vol.17 , pp. 1182-1188
    • Lombardino, J.G.1    Wiseman, E.H.2
  • 3
    • 9744244918 scopus 로고    scopus 로고
    • Optimization of protein kinase CK2 inhibitors derived from 4, 5,6,7-tetrabromobenzimidazole
    • M.A. Pagano, M. Andrzejewska, and M. Ruzzene Optimization of protein kinase CK2 inhibitors derived from 4, 5,6,7-tetrabromobenzimidazole J. Med. Chem. 47 2004 6239 6247
    • (2004) J. Med. Chem. , vol.47 , pp. 6239-6247
    • Pagano, M.A.1    Andrzejewska, M.2    Ruzzene, M.3
  • 4
    • 0032868495 scopus 로고    scopus 로고
    • N-Substituted-imidazoles as inhibitors of nitric oxide synthase: A preliminary screening
    • L. Salerno, V. Sorrenti, and F. Guerrera N-Substituted-imidazoles as inhibitors of nitric oxide synthase: a preliminary screening Pharmazie 54 1999 685 690
    • (1999) Pharmazie , vol.54 , pp. 685-690
    • Salerno, L.1    Sorrenti, V.2    Guerrera, F.3
  • 5
    • 0024383182 scopus 로고
    • Synthesis of 1-methyl-4-nitro-5-substituted imidazole and substituted imidazolothiazole derivatives as possible antiparasitic agents
    • A. Mukherjee, S. Kumar, M. Seth, and A.P. Bhaduri Synthesis of 1-methyl-4-nitro-5-substituted imidazole and substituted imidazolothiazole derivatives as possible antiparasitic agents Ind. J. Chem. B 28 1989 391 396
    • (1989) Ind. J. Chem. B , vol.28 , pp. 391-396
    • Mukherjee, A.1    Kumar, S.2    Seth, M.3    Bhaduri, A.P.4
  • 6
    • 33745875936 scopus 로고    scopus 로고
    • Synthesis and antifungal properties of some benzimidazole derivatives
    • G. Ayhan-Kilcigil, and N. Altanlar Synthesis and antifungal properties of some benzimidazole derivatives Turk. J. Chem. 30 2006 223 228
    • (2006) Turk. J. Chem. , vol.30 , pp. 223-228
    • Ayhan-Kilcigil, G.1    Altanlar, N.2
  • 7
    • 67549092062 scopus 로고    scopus 로고
    • Synthesis and antidepressant activity of N-substituted imidazole-5-caboxamides in forced swimming test model
    • F.H. Hadizadeh, V. Hosseinzadeh, M. Shariaty, and S.J. Kazemi Synthesis and antidepressant activity of N-substituted imidazole-5-caboxamides in forced swimming test model Pharm. Res. 7 2008 29 33
    • (2008) Pharm. Res. , vol.7 , pp. 29-33
    • Hadizadeh, F.H.1    Hosseinzadeh, V.2    Shariaty, M.3    Kazemi, S.J.4
  • 8
    • 67651163413 scopus 로고    scopus 로고
    • Synthesis and evaluation of anti-microbial and anti-tubercular activity of 2-styryl benzimidazoles
    • R.V. Shingalapur, K.M. Hosamani, and R.S. Keri Synthesis and evaluation of anti-microbial and anti-tubercular activity of 2-styryl benzimidazoles Eur. J. Med. Chem. 44 2009 4244 4248
    • (2009) Eur. J. Med. Chem. , vol.44 , pp. 4244-4248
    • Shingalapur, R.V.1    Hosamani, K.M.2    Keri, R.S.3
  • 9
    • 77954309331 scopus 로고    scopus 로고
    • Synthesis of 2-substituted-N-[4-(1-methyl-4, 5-diphenyl-1H-imidazole-2- yl)phenyl]acetamide derivatives and evaluation of their anticancer activity
    • Y. Ozkay, I. Iskar, Z. Incesu, and G.E. Akalin Synthesis of 2-substituted-N-[4-(1-methyl-4, 5-diphenyl-1H-imidazole-2-yl)phenyl]acetamide derivatives and evaluation of their anticancer activity Eur. J. Med. Chem. 45 2010 3320 3328
    • (2010) Eur. J. Med. Chem. , vol.45 , pp. 3320-3328
    • Ozkay, Y.1    Iskar, I.2    Incesu, Z.3    Akalin, G.E.4
  • 10
    • 77950519765 scopus 로고    scopus 로고
    • Antiviral activity of benzimidazole derivatives. II. Antiviral activity of 2-phenylbenzimidazole derivatives
    • M. Tonelli, M. Simone, B. Tasso, F. Novelli, and V. Biodo Antiviral activity of benzimidazole derivatives. II. Antiviral activity of 2-phenylbenzimidazole derivatives Bioorg. Med. Chem. 18 2010 2937 2953
    • (2010) Bioorg. Med. Chem. , vol.18 , pp. 2937-2953
    • Tonelli, M.1    Simone, M.2    Tasso, B.3    Novelli, F.4    Biodo, V.5
  • 11
    • 72049108895 scopus 로고    scopus 로고
    • Synthesis of substituted aryloxy alkyl and aryloxy aryl alkyl imidazoles as antileishmanial agents
    • K. Bhandari, N. Srinivas, and V.K. Marrapu Synthesis of substituted aryloxy alkyl and aryloxy aryl alkyl imidazoles as antileishmanial agents Bioorg. Med. Chem. Lett. 20 2010 291 293
    • (2010) Bioorg. Med. Chem. Lett. , vol.20 , pp. 291-293
    • Bhandari, K.1    Srinivas, N.2    Marrapu, V.K.3
  • 12
    • 57749116985 scopus 로고    scopus 로고
    • Aryloxy cyclohexyl imidazoles: A novel class of antileishmanial agents
    • N. Srinivas, S. Plane, N.S. Gupta, and K. Bhandari Aryloxy cyclohexyl imidazoles: a novel class of antileishmanial agents Bioorg. Med. Chem. Lett. 19 2009 324 327
    • (2009) Bioorg. Med. Chem. Lett. , vol.19 , pp. 324-327
    • Srinivas, N.1    Plane, S.2    Gupta, N.S.3    Bhandari, K.4
  • 14
    • 0942290524 scopus 로고    scopus 로고
    • Engineered films for display technologies
    • W.A.J. MacDonald Engineered films for display technologies Mat. Chem. 14 2004 4 10
    • (2004) Mat. Chem. , vol.14 , pp. 4-10
    • Macdonald, W.A.J.1
  • 15
    • 0031359868 scopus 로고    scopus 로고
    • Oxadiazoles and phenylquinoxalines s electron transport materials
    • J. Bettenhausen, M. Greczmiel, M. Jandke, and P. Strohriegl Oxadiazoles and phenylquinoxalines s electron transport materials Synth. Mat. 91 1997 223 228
    • (1997) Synth. Mat. , vol.91 , pp. 223-228
    • Bettenhausen, J.1    Greczmiel, M.2    Jandke, M.3    Strohriegl, P.4
  • 16
    • 38549173044 scopus 로고    scopus 로고
    • 2-symmetric chiral catalyst and its application in the catalytic asymmetric borane reduction of prochiral ketones
    • 2-symmetric chiral catalyst and its application in the catalytic asymmetric borane reduction of prochiral ketones Chirality 20 2008 110 114
    • (2008) Chirality , vol.20 , pp. 110-114
    • Zhou, Y.1    Wang, W.H.2    Dou, W.3    Tang, X.L.4    Liu, W.S.5
  • 17
    • 18844386480 scopus 로고    scopus 로고
    • Synthesis, optical and morphological characterization of soluble main chain 1,3,4-oxadiazole copolyarylethers-potential candidates for solar cells applications as electron acceptors
    • C.L. Chochos, G.K. Govaris, and F. Kakali Synthesis, optical and morphological characterization of soluble main chain 1,3,4-oxadiazole copolyarylethers-potential candidates for solar cells applications as electron acceptors Polymer 46 2005 4654 4663
    • (2005) Polymer , vol.46 , pp. 4654-4663
    • Chochos, C.L.1    Govaris, G.K.2    Kakali, F.3
  • 19
    • 40849117943 scopus 로고    scopus 로고
    • An efficient reagent system for the one-pot synthesis of 1, 2,4,5-tetrasubstituted imidazoles
    • B. Sadeghia, B.F. Mirjalili, and M.M. Hashemi An efficient reagent system for the one-pot synthesis of 1, 2,4,5-tetrasubstituted imidazoles Tetrahedron Lett. 49 2008 2575 2577
    • (2008) Tetrahedron Lett. , vol.49 , pp. 2575-2577
    • Sadeghia, B.1    Mirjalili, B.F.2    Hashemi, M.M.3
  • 20
    • 44649119225 scopus 로고    scopus 로고
    • Ytterbium perfluorooctanesulfonate as an efficient and recoverable catalyst for the synthesis of trisubstituted imidazoles
    • M. GuiShen, C. Cai, and W.B. Yi Ytterbium perfluorooctanesulfonate as an efficient and recoverable catalyst for the synthesis of trisubstituted imidazoles J. Fluorine Chem. 129 2008 541 544
    • (2008) J. Fluorine Chem. , vol.129 , pp. 541-544
    • Guishen, M.1    Cai, C.2    Yi, W.B.3
  • 22
    • 77951295528 scopus 로고    scopus 로고
    • Simple and efficient method for the synthesis of highly substituted imidazoles using zeolite-supported reagents
    • K. Sivakumar, A. Kathirvel, and A. Lalitha Simple and efficient method for the synthesis of highly substituted imidazoles using zeolite-supported reagents Tetrahedron Lett. 51 2010 3018 3021
    • (2010) Tetrahedron Lett. , vol.51 , pp. 3018-3021
    • Sivakumar, K.1    Kathirvel, A.2    Lalitha, A.3
  • 23
    • 77956341249 scopus 로고    scopus 로고
    • DABCO as a mild and efficient catalytic system for the synthesis of highly substituted imidazoles via multi-component condensation strategy
    • M.S. Narayana, B. Madhav, and Y.V.D. Nageswar DABCO as a mild and efficient catalytic system for the synthesis of highly substituted imidazoles via multi-component condensation strategy Tetrahedron Lett. 51 2010 5252 5257
    • (2010) Tetrahedron Lett. , vol.51 , pp. 5252-5257
    • Narayana, M.S.1    Madhav, B.2    Nageswar, Y.V.D.3
  • 24
    • 68849118191 scopus 로고    scopus 로고
    • Synthesis and optical behaviors of 2-(9-phenanthrenyl)-2-(9-anthryl)-, and 2-(1-pyrenyl)-1-alkylimidazole homologues
    • Y.N. Yana, D.Y. Lina, and W.L. Panb Synthesis and optical behaviors of 2-(9-phenanthrenyl)-2-(9-anthryl)-, and 2-(1-pyrenyl)-1-alkylimidazole homologues Spectrochim. Acta A 74 2009 233 242
    • (2009) Spectrochim. Acta A , vol.74 , pp. 233-242
    • Yana, Y.N.1    Lina, D.Y.2    Panb, W.L.3
  • 25
    • 77957839776 scopus 로고    scopus 로고
    • Luminescent properties of some imidazole and oxazole based heterocycles: Synthesis, structure and substituent effects
    • A.O. Eseola, W. Lib, and W.H. Sun Luminescent properties of some imidazole and oxazole based heterocycles: synthesis, structure and substituent effects Dyes Pigments 88 2011 262 273
    • (2011) Dyes Pigments , vol.88 , pp. 262-273
    • Eseola, A.O.1    Lib, W.2    Sun, W.H.3
  • 26
    • 77950866074 scopus 로고    scopus 로고
    • The synthesis and optical properties of novel 1,3,4-oxadiazole derivatives containing an imidazole unit
    • Y.N. Yan, W.L. Pan, and H.C. Song The synthesis and optical properties of novel 1,3,4-oxadiazole derivatives containing an imidazole unit Dyes Pigments 86 2010 249 258
    • (2010) Dyes Pigments , vol.86 , pp. 249-258
    • Yan, Y.N.1    Pan, W.L.2    Song, H.C.3
  • 27
    • 0019222537 scopus 로고
    • Phenotypic resistance to miconazole and amphotericin B in Candida albicans
    • E.F. Gale, A.M. Johnson, D. Kerridge, and F. Wayman Phenotypic resistance to miconazole and amphotericin B in Candida albicans Gen. Microbiol. 117 1980 535 538
    • (1980) Gen. Microbiol. , vol.117 , pp. 535-538
    • Gale, E.F.1    Johnson, A.M.2    Kerridge, D.3    Wayman, F.4
  • 28
    • 77953984445 scopus 로고    scopus 로고
    • Synthesis and antibacterial evaluation of 2-substituted-4,5-diphenyl-N- alkyl imidazole derivatives
    • A.K. Jain, V. Ravichandran, M. Sisodiya, and R.K. Agrawal Synthesis and antibacterial evaluation of 2-substituted-4,5-diphenyl-N-alkyl imidazole derivatives Asian Pac. J. Trop. Med. 2010 471 474
    • (2010) Asian Pac. J. Trop. Med. , pp. 471-474
    • Jain, A.K.1    Ravichandran, V.2    Sisodiya, M.3    Agrawal, R.K.4
  • 29
    • 84865446394 scopus 로고    scopus 로고
    • An expeditious regioselective synthesis of novel bioactive indole-substituted chromene derivatives via one-pot three-component reaction
    • R. Hosseinnia, M. Mamaghani, K. Tabatabaeian, F. Shirini, and M. Rassa An expeditious regioselective synthesis of novel bioactive indole-substituted chromene derivatives via one-pot three-component reaction Bioorg. Med. Chem. Lett. 22 2012 5956 5960
    • (2012) Bioorg. Med. Chem. Lett. , vol.22 , pp. 5956-5960
    • Hosseinnia, R.1    Mamaghani, M.2    Tabatabaeian, K.3    Shirini, F.4    Rassa, M.5
  • 30
    • 84859005818 scopus 로고    scopus 로고
    • An efficient regioselective sonochemical synthesis of novel 4-aryl-3-methyl-4,5-dihydro-1H-pyrazolo[3,4-b]pyridin-6(7H)-ones
    • A. Azimi Roshan, M. Mamaghani, N.O. Mahmoodi, and F. Shirini An efficient regioselective sonochemical synthesis of novel 4-aryl-3-methyl-4,5-dihydro-1H- pyrazolo[3,4-b]pyridin-6(7H)-ones Chin. Chem. Lett. 23 2012 399 402
    • (2012) Chin. Chem. Lett. , vol.23 , pp. 399-402
    • Azimi Roshan, A.1    Mamaghani, M.2    Mahmoodi, N.O.3    Shirini, F.4
  • 31
    • 41549151623 scopus 로고    scopus 로고
    • Base supported ionic liquid-like phases as catalysts for the batch and continuous-flow Henry reaction
    • M.I. Burguete, H. Erytropel, E.G. Verdugo, S.V. Luis, and V. Sans Base supported ionic liquid-like phases as catalysts for the batch and continuous-flow Henry reaction Green Chem. 10 2008 401 407
    • (2008) Green Chem. , vol.10 , pp. 401-407
    • Burguete, M.I.1    Erytropel, H.2    Verdugo, E.G.3    Luis, S.V.4    Sans, V.5
  • 32
    • 58049189252 scopus 로고    scopus 로고
    • Ultrasounds assisted reactions of steroid analogous of anticipated biological activities, Mangalagiu II
    • V. Bejan, and C. Moldoveanu Ultrasounds assisted reactions of steroid analogous of anticipated biological activities, Mangalagiu II Ultrason. Sonochem. 16 2009 312 315
    • (2009) Ultrason. Sonochem. , vol.16 , pp. 312-315
    • Bejan, V.1    Moldoveanu, C.2


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