Highly Efficient, One-Pot, Solvent-Free Synthesis of Highly Substituted Imidazoles Using Molecular Iodine as Catalyst

Yi Ming Ren; Chun Cai

doi:10.4028/www.scientific.net/AMR.396-398.1871

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Highly Efficient, One-Pot, Solvent-Free Synthesis of Highly Substituted Imidazoles Using Molecular Iodine as Catalyst
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HomeAdvanced Materials ResearchAdvanced Materials Research Vols. 396-398Highly Efficient, One-Pot, Solvent-Free Synthesis...

Highly Efficient, One-Pot, Solvent-Free Synthesis of Highly Substituted Imidazoles Using Molecular Iodine as Catalyst

Abstract:

Highly efficient, one-pot synthesis of 2,4,5-trisubstituted and 1,2,4,5-tetrasubstituted imidazoles under solvent-free conditions using molecular iodine as the catalyst is described with excellent product yields.

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Advanced Materials Research (Volumes 396-398)

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1871-1874

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https://doi.org/10.4028/www.scientific.net/AMR.396-398.1871

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Online since:

November 2011

Authors:

Yi Ming Ren, Chun Cai

Keywords:

1,2,4,5-Tetrasubstituted Imidazoles, 2,4,5-Trisubstituted Imidazoles, Molecular Iodine, Solvent-Free

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References

[1] J.W. Blank, G.J. Durant, J.C. Emmett and C.R. Ganellin: Nature Vol. 248 (1974), p.65

Google Scholar

[2] P.W. Erhardt: J. Med. Chem. Vol. 30 (1987), p.231

Google Scholar

[3] B.E. Tomczuk, C.R.Jr. Taylor, L.M. Moses, D.B. Sutherland, Y.S. Lo, D.N. Johnson, W.B. Kinnier and B.F. Kilpatrick: J. Med. Chem. Vol. 34 (1991), p.2993

Google Scholar

[4] J.S. Kim, B. Gatto, C. Yu, A. Liu, L.F. Liu and E.J. LaVoie: J. Med. Chem. Vol. 39 (1996), p.992

Google Scholar

[5] T. Roth, M.L. Morningstar, P.L. Boyer, S.H. Hughes, R.W.Jr. Buckheit and C.J. Michejda: J. Med. Chem. Vol. 40 (1997), p.4199

Google Scholar

[6] M. Misono: Chem. Commun. Vol. 37 (2001), p.1141

Google Scholar

[7] U. Ucucu, N.G. Karaburun and I. Iskdag: Il Farmaco Vol. 56 (2001), p.285

Google Scholar

[8] D.A. Evans and K.M. Lundy: J. Am. Chem. Soc. Vol. 114 (1992), p.1495

Google Scholar

[9] A. Shaabani and A. Rahamati: J. Mol. Catal. A: Chem. Vol. 249 (2006), p.246

Google Scholar

[10] M.M. Heravi, K. Bakhtiari, H.A. Oskooie and S. Taheri: J. Mol. Catal. A: Chem. Vol. 263 (2007), p.279

Google Scholar

[11] M. Kidwai, P. Mothsra, V. Bansal, R.K. Somvanshi, A.S. Ethayathulla, S. Dey and T.P. Singh: J. Mol. Catal. A: Chem. Vol. 265 (2007), p.177

Google Scholar

[12] S. Balalaie, M.M. Hashemi and M. Akhbari: Tetrahedron Lett. Vol. 44 (2003), p.1709

Google Scholar

[13] A.R. Karimi, Z. Alimohammadi, J. Azizian, A.A. Mohammadi and M.R. Mohammadizadeh: Catal. Commun. Vol. 7 (2006), p.728

Google Scholar

[14] M. Kidwai and P.A. Mothsra: Tetrahedron Lett. Vol. 47 (2006), p.5029

Google Scholar

[15] L. Nagarapu, S. Apuri and S. Kantevari: J. Mol. Catal. A: Chem. Vol. 266 (2007), p.104

Google Scholar

[16] M.M. Heravi, F. Derikvand and F.F. Bamoharram: J. Mol. Catal. A: Chem. Vol. 263 (2007), p.112.

Google Scholar

[17] M. Ishihara and H. Togo: Tetrahedron Vol. 63 (2007), p.1474

Google Scholar

[18] J.W.J. Bosco, A. Agrahari and A.K. Saikia: Tetrahedron Lett. Vol. 47 (2006), p.4065

Google Scholar

[19] W. Rao, A.H.L. Tay, P.J. Goh, J.M.L. Choy, J.K. Ke and P.W.H. Chan: Tetrahedron Lett. Vol. 49 (2008), p.122.

Google Scholar

[20] F. Toda and K. Tanaka: Chem. Rev. Vol. 100 (2000), p.1025

Google Scholar

[21] A.R. Karimi, Z. Alimohammadi, J. Azizian, A.A. Mohammadi and M.R. Mohammadizadeh: Catal. Commun. Vol. 7 (2006), p.728

Google Scholar

[22] S. Kantevari, S.V.N. Vuppalapati, O. Biradar and L. Nagarapu: J. Mol. Catal. A: Chem. Vol. 266 (2007), p.109

Google Scholar

[23] Y.M. Ren and C. Cai: J. Chem. Res-S. Vol. 35 (2010), p.133

Google Scholar