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Volumn 90, Issue 2, 2012, Pages 195-198

Highly efficient one-pot synthesis of trisubstituted imidazoles under catalyst-free conditions

Author keywords

Aldehyde; Atom economic; Benzil; Catalyst free; Imidazole; Solvent effect

Indexed keywords

AMMONIUM ACETATE; BENZIL; CATALYST FREE; HIGH YIELD; IMIDAZOLE; ONE-POT SYNTHESIS; SCALABLE SYNTHESIS; SOLVENT EFFECT;

EID: 84856337526     PISSN: 00084042     EISSN: None     Source Type: Journal    
DOI: 10.1139/v11-141     Document Type: Article
Times cited : (21)

References (42)
  • 2
    • 0016260535 scopus 로고
    • 10.1021/cr60290a003
    • b Sundberg R. Martin R. B. Chem. Rev. 1974, 74 (4), 471. 10.1021/cr60290a003
    • (1974) Chem. Rev. , vol.74 , Issue.4 , pp. 471
    • Sundberg, R.1    Martin, R.B.2
  • 6
    • 1842679186 scopus 로고    scopus 로고
    • Design, Synthesis, and Biological Evaluation of Substituted 2-Cyclohexyl-4-phenyl-1H-imidazoles: Potent and Selective Neuropeptide Y Y5-Receptor Antagonists
    • DOI 10.1021/jm030490g
    • b Blum C. A. Zheng X. De Lombaert S. J. Med. Chem. 2004, 47 (9), 2318. 10.1021/jm030490g (Pubitemid 38478855)
    • (2004) Journal of Medicinal Chemistry , vol.47 , Issue.9 , pp. 2318-2325
    • Blum, C.A.1    Zheng, X.2    De Lombaert, S.3
  • 7
    • 0347417134 scopus 로고    scopus 로고
    • 10.1021/cr980032t
    • a Welton T. Chem. Rev. 1999, 99 (8), 2071. 10.1021/cr980032t
    • (1999) Chem. Rev. , vol.99 , Issue.8 , pp. 2071
    • Welton, T.1
  • 9
    • 34547338866 scopus 로고    scopus 로고
    • N-Heterocyclic Carbenes in Transition Metal Catalysis
    • Springer: Berlin
    • Glorius, F. N-Heterocyclic Carbenes in Transition Metal Catalysis. In Topics in Organometallic Chemistry; Springer: Berlin, 2007; Vol. 2, pp 1-218.
    • (2007) Topics in Organometallic Chemistry , vol.2 , pp. 1-218
    • Glorius, F.1
  • 12
    • 34250645840 scopus 로고    scopus 로고
    • 10.1002/asia.200600418
    • Kamijo S. Yamamoto Y. Chem. Asian J. 2007, 2 (5), 568. 10.1002/asia.200600418
    • (2007) Chem. Asian J. , vol.2 , Issue.5 , pp. 568
    • Kamijo, S.1    Yamamoto, Y.2
  • 13
    • 0028600543 scopus 로고
    • 10.1021/jo00103a021
    • a Little T. L. Webber S. E. J. Org. Chem. 1994, 59 (24), 7299. 10.1021/jo00103a021
    • (1994) J. Org. Chem. , vol.59 , Issue.24 , pp. 7299
    • Little, T.L.1    Webber, S.E.2
  • 17
    • 0032568905 scopus 로고    scopus 로고
    • A one-pot synthesis of 1-(2,2,6,6-tetramethyl-4-piperidinyl)-4-(4- fluorophenyl)-5-(2-amino-4-pyrimidinyl)-imidazole: A potent inhibitor of P38 MAP kinase
    • DOI 10.1021/jo980248v
    • b Sisko J. J. Org. Chem. 1998, 63 (13), 4529. 10.1021/jo980248v (Pubitemid 28334271)
    • (1998) Journal of Organic Chemistry , vol.63 , Issue.13 , pp. 4529-4531
    • Sisko, J.1
  • 18
    • 0036694454 scopus 로고    scopus 로고
    • and references therein. 10.1351/pac200274081349
    • c Sisko J. Mellinger M. Pure Appl. Chem. 2002, 74 (8), 1349. and references therein. 10.1351/pac200274081349
    • (2002) Pure Appl. Chem. , vol.74 , Issue.8 , pp. 1349
    • Sisko, J.1    Mellinger, M.2
  • 19
    • 12344263141 scopus 로고    scopus 로고
    • A novel three-component one-pot synthesis of 1H-imidazol-4-yl-pyridines
    • DOI 10.1021/ol0480269
    • d Illgen K. Nerdinger S. Behnke D. Friedrich A. Org. Lett. 2005, 7 (1), 39. 10.1021/ol0480269 (Pubitemid 40138306)
    • (2005) Organic Letters , vol.7 , Issue.1 , pp. 39-42
    • Illgen, K.1    Nerdinger, S.2    Behnke, D.3    Friedrich, C.4
  • 22
    • 33744996505 scopus 로고    scopus 로고
    • A one-pot synthesis of 1,2,4,5-tetraarylimidazoles using molecular iodine as an efficient catalyst
    • DOI 10.1016/j.tetlet.2006.05.097, PII S0040403906010318
    • c Kidwai M. Mothsra P. Tetrahedron Lett. 2006, 47 (29), 5029. 10.1016/j.tetlet.2006.05.097 (Pubitemid 43867632)
    • (2006) Tetrahedron Letters , vol.47 , Issue.29 , pp. 5029-5031
    • Kidwai, M.1    Mothsra, P.2
  • 23
    • 41549093210 scopus 로고    scopus 로고
    • 4 as a powerful Brönsted acidic ionic liquid
    • DOI 10.1139/V08-009
    • d Khosropour A. R. Can. J. Chem. 2008, 86 (3), 264. 10.1139/v08-009 (Pubitemid 351466613)
    • (2008) Canadian Journal of Chemistry , vol.86 , Issue.3 , pp. 264-269
    • Khosropour, A.R.1
  • 26
    • 3242730586 scopus 로고    scopus 로고
    • Microwave-assisted synthesis of 2,4,5-Triaryl-Imidazole; a novel thermally induced N-hydroxyimidazole N-O bond cleavage
    • DOI 10.1021/ol049124x
    • g Sparks R. B. Combs A. P. Org. Lett. 2004, 6 (14), 2473. 10.1021/ol049124x (Pubitemid 38952566)
    • (2004) Organic Letters , vol.6 , Issue.14 , pp. 2473-2475
    • Sparks, R.B.1    Combs, A.P.2
  • 35
    • 0342961000 scopus 로고    scopus 로고
    • Synthesis and analgesic activity of some 1-benzyl-2-substituted-4,5- diphenyl-1H-imidazole derivatives
    • DOI 10.1016/S0014-827X(01)01076-X, PII S0014827X0101076X
    • p Uçucu U. Karaburun N. G. Işikdaǧ I. Il Farmaco 2001, 56 (4), 285. 10.1016/S0014-827X(01)01076-X (Pubitemid 32463311)
    • (2001) Farmaco , vol.56 , Issue.4 , pp. 285-290
    • Ucucu, U.1    Karaburun, N.G.2    Isikdag, I.3
  • 37
    • 1642528348 scopus 로고    scopus 로고
    • New method for the synthesis of diversely functionalized imidazoles from N-acylated α-aminonitriles
    • DOI 10.1021/ol036423y
    • b Zhong Y. L. Lee J. Reamer R. A. Askin D. Org. Lett. 2004, 6 (6), 929. 10.1021/ol036423y (Pubitemid 38402664)
    • (2004) Organic Letters , vol.6 , Issue.6 , pp. 929-931
    • Zhong, Y.-L.1    Lee, J.2    Reamer, R.A.3    Askin, D.4
  • 39
    • 1842428974 scopus 로고    scopus 로고
    • 10.1021/om0341505
    • a Azizi N. Saidi M. R. Organometallics 2004, 23 (6), 1457. 10.1021/om0341505
    • (2004) Organometallics , vol.23 , Issue.6 , pp. 1457
    • Azizi, N.1    Saidi, M.R.2
  • 40
    • 24044486238 scopus 로고    scopus 로고
    • Highly chemoselective addition of amines to epoxides in water
    • DOI 10.1021/ol051220q
    • b Azizi N. Saidi M. R. Org. Lett. 2005, 7 (17), 3649. 10.1021/ol051220q (Pubitemid 41224543)
    • (2005) Organic Letters , vol.7 , Issue.17 , pp. 3649-3651
    • Azizi, N.1    Saidi, M.R.2
  • 42
    • 33744758029 scopus 로고    scopus 로고
    • Highly efficient one-pot three-component Mannich reaction in water catalyzed by heteropoly acids
    • DOI 10.1021/ol060498v
    • d Azizi N. Torkiyan L. Saidi M. R. Org. Lett. 2006, 8 (10), 2079. 10.1021/ol060498v (Pubitemid 43823615)
    • (2006) Organic Letters , vol.8 , Issue.10 , pp. 2079-2082
    • Azizi, N.1    Torkiyan, L.2    Saidi, M.R.3


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