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Volumn 131, Issue 3-4, 2009, Pages 552-559

Wells-dawson heteropolyacid: An efficient recyclable catalyst for the synthesis of benzimidazoles under microwave condition

Author keywords

Benzimidazole; Heteropolyacid H 6P2W18O62 24H2O; Microwave irradiation; O Phenylenediamines; Wells Dawson

Indexed keywords

BENZIMIDAZOLE; BENZIMIDAZOLE DERIVATIVES; BENZIMIDAZOLES; CATALYTIC ACTIVITY; ENVIRONMENTALLY-FRIENDLY; HETEROGENEOUS REACTIONS; HETEROPOLY ACIDS; MICROWAVE CONDITIONS; O-PHENYLENEDIAMINES; PHENOXYACETIC ACID; RECYCLABLE CATALYST; WELLS-DAWSON;

EID: 70349224432     PISSN: 1011372X     EISSN: 1572879X     Source Type: Journal    
DOI: 10.1007/s10562-009-9966-2     Document Type: Article
Times cited : (16)

References (42)
  • 1
    • 0035742524 scopus 로고    scopus 로고
    • 10.1351/pac200173010103 1:CAS:528:DC%2BD3MXjtVeltb4%3D
    • JH Clark 2001 Pure Appl Chem 73 103 10.1351/pac200173010103 1:CAS:528:DC%2BD3MXjtVeltb4%3D
    • (2001) Pure Appl Chem , vol.73 , pp. 103
    • Clark, J.H.1
  • 3
    • 0034583293 scopus 로고    scopus 로고
    • 10.1351/pac200072071305 1:CAS:528:DC%2BD3cXotFKqs7s%3D
    • M Misono I Ono G Koyano A Aoshima 2000 Pure Appl Chem 72 1305 10.1351/pac200072071305 1:CAS:528:DC%2BD3cXotFKqs7s%3D
    • (2000) Pure Appl Chem , vol.72 , pp. 1305
    • Misono, M.1    Ono, I.2    Koyano, G.3    Aoshima, A.4
  • 6
    • 0035945983 scopus 로고    scopus 로고
    • A short synthesis of phenanthro[2,3-d]imidazoles from dehydroabietic acid. Application of the methodology as a convenient route to benzimidazoles
    • DOI 10.1016/S0040-4020(00)01158-3, PII S0040402000011583
    • T Fonseca B Gigante TL Gilchrist 2001 Tetrahedron 57 1793 10.1016/S0040-4020(00)01158-3 1:CAS:528:DC%2BD3MXhsFGhsb0%3D (Pubitemid 32181825)
    • (2001) Tetrahedron , vol.57 , Issue.9 , pp. 1793-1799
    • Fonseca, T.1    Gigante, B.2    Gilchrist, T.L.3
  • 7
    • 26244450484 scopus 로고    scopus 로고
    • Microwave-assisted synthesis of 1-aryl-1H-indazoles via one-pot two-step Cu-catalyzed intramolecular N-arylation of arylhydrazones
    • DOI 10.1016/j.tetlet.2005.08.143, PII S0040403905019076
    • C Pabba HJ Wang SR Mulligan ZJ Chen TM Stark BT Gregg 2005 Tetrahedron Lett 46 7553 10.1016/j.tetlet.2005.08.143 1:CAS:528:DC%2BD2MXhtVCksrzE (Pubitemid 41411856)
    • (2005) Tetrahedron Letters , vol.46 , Issue.44 , pp. 7553-7557
    • Pabba, C.1    Wang, H.-J.2    Mulligan, S.R.3    Chen, Z.-J.4    Stark, T.M.5    Gregg, B.T.6
  • 10
    • 0032499283 scopus 로고    scopus 로고
    • Design, synthesis, and antiviral evaluations of 1-(substituted benzyl)- 2-substituted-5,6-dichlorobenzimidazoles as nonnucleoside analogues of 2,5,6- trichloro-1-(β-D-ribofuranosyl)benzimidazole
    • DOI 10.1021/jm970559i
    • AR Porcari RV Devivar LS Kucera JC Drach LB Townsend 1998 J Med Chem 41 1252 10.1021/jm970559i 1:CAS:528:DyaK1cXhvFyhsro%3D (Pubitemid 28208180)
    • (1998) Journal of Medicinal Chemistry , vol.41 , Issue.8 , pp. 1252-1262
    • Porcari, A.R.1    Devivar, R.V.2    Kucera, L.S.3    Drach, J.C.4    Townsend, L.B.5
  • 12
    • 0017915202 scopus 로고
    • 10.1016/S0065-3527(08)60775-7 1:CAS:528:DyaE1cXksFeqsLY%3D
    • I Tamm PB Sehgal 1978 Adv Virus Res 22 187 10.1016/S0065-3527(08)60775-7 1:CAS:528:DyaE1cXksFeqsLY%3D
    • (1978) Adv Virus Res , vol.22 , pp. 187
    • Tamm, I.1    Sehgal, P.B.2
  • 13
    • 0040482632 scopus 로고
    • I Tamm 1957 Science 126 1235
    • (1957) Science , vol.126 , pp. 1235
    • Tamm, I.1
  • 17
    • 0030480485 scopus 로고    scopus 로고
    • Synthesis and angiotensin II receptor antagonistic activities of benzimidazole derivatives bearing acidic heterocycles as novel tetrazole bioisosteres
    • DOI 10.1021/jm960547h
    • Y Kohara K Kubo E Imamiya T Wada T Naka Y Inada 1996 J Med Chem 39 5228 10.1021/jm960547h 1:CAS:528:DyaK28XntFaqsrY%3D (Pubitemid 27010313)
    • (1996) Journal of Medicinal Chemistry , vol.39 , Issue.26 , pp. 5228-5235
    • Kohara, Y.1    Kubo, K.2    Imamiya, E.3    Wada, T.4    Inada, Y.5    Naka, T.6
  • 20
    • 0346499274 scopus 로고    scopus 로고
    • 10.1021/ja030196d 1:CAS:528:DC%2BD3sXpvVKntLY%3D
    • T Fekner J Gallucci MK Chan 2004 J Am Chem Soc 126 223 10.1021/ja030196d 1:CAS:528:DC%2BD3sXpvVKntLY%3D
    • (2004) J Am Chem Soc , vol.126 , pp. 223
    • Fekner, T.1    Gallucci, J.2    Chan, M.K.3
  • 21
    • 33748861128 scopus 로고    scopus 로고
    • Rapid one-pot preparation of 2-substituted benzimidazoles from esters using microwave conditions
    • DOI 10.1080/00397910600764204, PII XU9436806U532354
    • X Jing Q Zhu F Xu X Ren D Li C Yan 2006 Synth Commun 36 2597 10.1080/00397910600764204 1:CAS:528:DC%2BD28XhtV2ht7nI (Pubitemid 44423097)
    • (2006) Synthetic Communications , vol.36 , Issue.18 , pp. 2597-2601
    • Jing, X.1    Zhu, Q.2    Xu, F.3    Ren, X.4    Li, D.5    Yan, C.6
  • 22
    • 2342454576 scopus 로고    scopus 로고
    • 2O promoted one-pot expeditious and convenient synthesis of 2-substituted benzimidazoles and 3,1,5-benzoxadiazepines
    • DOI 10.1016/j.tetlet.2004.03.117, PII S0040403904006665
    • VK Tandon M Kumar 2004 Tetrahedron Lett 45 4185 10.1016/j.tetlet.2004.03. 117 1:CAS:528:DC%2BD2cXjs1ertL4%3D (Pubitemid 38581841)
    • (2004) Tetrahedron Letters , vol.45 , Issue.21 , pp. 4185-4187
    • Tandon, V.K.1    Kumar, M.2
  • 23
    • 0035059764 scopus 로고    scopus 로고
    • Nouvelle voie de synthése des 2- trifluorométhylarylimidazoles sur montmorillonite K10 en 'milieu sec' sous micro-onde
    • DOI 10.1016/S0040-4020(00)00992-3, PII S0040402000009923
    • K Bougrin A Loupy A Petit B Daou M Soufiaoui 2001 Tetrahedron 57 163 10.1016/S0040-4020(00)00992-3 1:CAS:528:DC%2BD3MXpsVGqsQ%3D%3D (Pubitemid 32367854)
    • (2001) Tetrahedron , vol.57 , Issue.1 , pp. 163-168
    • Bougrin, K.1    Loupy, A.2    Petit, A.3    Daou, B.4    Soufiaoui, M.5
  • 25
    • 24044521615 scopus 로고    scopus 로고
    • Rapid one-pot preparation of 2-substituted benzimidazoles from 2-nitroanilines using microwave conditions
    • DOI 10.1016/j.tetlet.2005.07.130, PII S0040403905016503
    • DS VanVliet P Gillespie JJ Scicinski 2005 Tetrahedron Lett 46 6741 10.1016/j.tetlet.2005.07.130 1:CAS:528:DC%2BD2MXpt1aqurw%3D (Pubitemid 41213301)
    • (2005) Tetrahedron Letters , vol.46 , Issue.39 , pp. 6741-6743
    • VanVliet, D.S.1    Gillespie, P.2    Scicinski, J.J.3
  • 26
    • 33845641679 scopus 로고    scopus 로고
    • Zeolite-catalyzed environmentally friendly synthesis of benzimidazole derivatives
    • DOI 10.1080/00397910600943865, PII V84L2JG28700UJ44
    • A Hegedus Z Hell A Potor 2006 Synth Commun 36 3625 10.1080/ 00397910600943865 1:CAS:528:DC%2BD2sXmslSitw%3D%3D (Pubitemid 44948985)
    • (2006) Synthetic Communications , vol.36 , Issue.23 , pp. 3625-3630
    • Hegedus, A.1    Hell, Z.2    Potor, A.3
  • 28
    • 33745008887 scopus 로고    scopus 로고
    • 10.1002/jhet.5570430338 1:CAS:528:DC%2BD28XlvVejs7o%3D
    • P Sun Z Hu 2006 J Heterocycl Chem 43 773 10.1002/jhet.5570430338 1:CAS:528:DC%2BD28XlvVejs7o%3D
    • (2006) J Heterocycl Chem , vol.43 , pp. 773
    • Sun, P.1    Hu, Z.2
  • 30
    • 33645783037 scopus 로고    scopus 로고
    • 10.1134/S1070428006030201 1:CAS:528:DC%2BD28XjtlCitbg%3D
    • RR Nagawade DB Shinde 2006 Rus J Org Chem 42 453 10.1134/ S1070428006030201 1:CAS:528:DC%2BD28XjtlCitbg%3D
    • (2006) Rus J Org Chem , vol.42 , pp. 453
    • Nagawade, R.R.1    Shinde, D.B.2
  • 32
    • 33846845982 scopus 로고    scopus 로고
    • 10.1016/j.jfluchem.2007.01.009 1:CAS:528:DC%2BD2sXhsF2gt7o%3D
    • MG Shen C Cai 2007 J Fluorine Chem 128 232 10.1016/j.jfluchem.2007.01.009 1:CAS:528:DC%2BD2sXhsF2gt7o%3D
    • (2007) J Fluorine Chem , vol.128 , pp. 232
    • Shen, M.G.1    Cai, C.2
  • 33
    • 10644251783 scopus 로고    scopus 로고
    • 3 as catalyst under solvent-free conditions
    • DOI 10.1081/SCC-200039340
    • L Wang J Sheng H Tian C Qian 2004 Synth Commun 34 4265 10.1081/SCC-200039340 1:CAS:528:DC%2BD2cXpvFKrs74%3D (Pubitemid 39657514)
    • (2004) Synthetic Communications , vol.34 , Issue.23 , pp. 4265-4272
    • Wang, L.1    Sheng, J.2    Tian, H.3    Qian, C.4
  • 36
    • 0033444261 scopus 로고    scopus 로고
    • 10.1039/a808223e 1:CAS:528:DyaK1MXit1ylsbo%3D
    • S Varma 1999 Green Chem 1 43 10.1039/a808223e 1:CAS:528: DyaK1MXit1ylsbo%3D
    • (1999) Green Chem , vol.1 , pp. 43
    • Varma, S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.