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Journal
2008 | 6 | 4 | 622-626
Article title

Ionic liquid promoted synthesis of bis(indolyl) methanes

Content
Title variants
Languages of publication
EN
Abstracts
EN
1-benzyl-3-methyl imidazolium hydrogen sulphate [bnmim][HSO4] was found to be an effective catalyst for the condensation reaction of indoles and derivatives with benzaldehydes in microwave irradiation with lower reaction time and higher yields to give bis(indolyl) methanes. [...]
Publisher

Journal
Year
Volume
6
Issue
4
Pages
622-626
Physical description
Dates
published
1 - 12 - 2008
online
28 - 10 - 2008
Contributors
  • Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad (M.S.), 431004, India
author
  • Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad (M.S.), 431004, India
author
  • Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad (M.S.), 431004, India
References
  • [1] T. Welton, Chem. Rev. 99, 2071 (1999) http://dx.doi.org/10.1021/cr980032t[Crossref]
  • [2] P. Wasserscheid and W. Keim, Angew. Chem. Int. Ed. 39, 3772 (2000) http://dx.doi.org/10.1002/1521-3773(20001103)39:21<3772::AID-ANIE3772>3.0.CO;2-5[Crossref]
  • [3] R. Sheldon, Chem. Commun. 2399 (2001) [Crossref]
  • [4] C.O. Kappe, Tetrahedron 49, 6937 (1993) and references cited therein http://dx.doi.org/10.1016/S0040-4020(01)87971-0[Crossref]
  • [5] J. G. Huddleston, A. E. Visser, W. M. Reichert, H. D. Willauer, G. A. Broker and R. D. Rogers, Green Chem. 3, 156 (2001) http://dx.doi.org/10.1039/b103275p[Crossref]
  • [6] S. Lee, J. H. Park, J. Kang and J. K. Lee, Chem. Commun. 1698 (2001) [Crossref]
  • [7] S. Csihony, C. Fischmeister, C. Bruneau, I. T. Horvath and P. H. Dixneuf, New J. Chem. 11, 1667 (2002) http://dx.doi.org/10.1039/b205920g[Crossref]
  • [8] (a) T. Fischer, A. Sethi, T. Welton, J. Woolf, Tetrahedron Lett. 40, 793 (1999); (b) Z. Baan, Z. Finta, G. Keglevich and I. Hermecz, Tetrahedron Lett. 46, 6203 (2005) [Crossref]
  • [9] A. Agarwal, N. L. Lancaster, A. R. Sethi and T. Welton, Green Chem. 5, 517 (2002) http://dx.doi.org/10.1039/b206472c[Crossref]
  • [10] R.S. Varma and V.V. Namboodiri, Pure Appl. Chem. 73, 1309 (2001) http://dx.doi.org/10.1351/pac200173081309[Crossref]
  • [11] J. Fraga-Dubreuil, J. K. Bourahla, M. Rahmouni, J. P. Bazureau and J. Hamelin, Catal. Commun. 3, 185 (2002) http://dx.doi.org/10.1016/S1566-7367(02)00087-0[Crossref]
  • [12] M.K. Potdar, S.S. Mohile and M.M. Salunkhe, Tetrahedron Lett. 42, 9285 (2001) http://dx.doi.org/10.1016/S0040-4039(01)02041-X[Crossref]
  • [13] (a) T. Osawa and M. Namiki, Tetrahedron Lett. 24, 4719 (1983); (b) J.K. Porter, C.W. Bacon, J.D. Robbin, D.S. Himmelsbach and H.C. Higman, J Agric Food Chem. 25, 88 (1977); (c) T.R. Garbe, M. Kobayashi, N. Shimizu, N. Takesue, M. Ozawa and H. Yukawa, J Nat Prod. 63, 596 (2000)
  • [14] (a) G.W. Gribble, In comprehensive Heterocyclic Chemistry, 2nd ed. (Pergamon Pres: New York, 1996) 202; (b) V. Snieckus, In The Alkaloids (Academic Press: New York, 1998) 11
  • [15] C. Hong, G.L. Firestone, L.F. Bjeldanes, Biochem. Pharmaco 63, 1085 (2002) http://dx.doi.org/10.1016/S0006-2952(02)00856-0[Crossref]
  • [16] X. Ge, S. Yannai, G. Rennert, N. Gruener and F. A. Fares, Biochem. Biophys. Res. Commun. 228, 153 (1996) http://dx.doi.org/10.1006/bbrc.1996.1631[Crossref]
  • [17] (a) C. Lin, J. Hsu, M.N.V. Sastry, H. Fang, Z. Tu, J. Liu and Y. Ching-Fa, Tetrahedron, 61, 11751 (2005); (b) G. Bartoli, M. Bartolacci, M. Bosco, G. Foglia, A. Giuliani, E. Mareantoni, L. Sambri and E. Torregiani, J. Org. Chem. 68, 4594 (2003)
  • [18] P. Anastas and J. C. Warner, Green chemistry, theory and practice (Oxford, UK, 1998)
  • [19] L. M. Wang, J. W. Han, H. Tian, J. Sheng, Z. Y. Fan and X. P. Tang, Synlett 337 (2005) [Crossref]
  • [20] G. V. M. Sharma, J. J. Reddy, P. S. Lakshmi and P. R. Krishna, Tetrahedron Lett. 45, 7729 (2004) http://dx.doi.org/10.1016/j.tetlet.2004.08.084[Crossref]
  • [21] B. P. Bandgar, S. V. Bettigeri and N. S. Joshi, Monatsh. Chem. 135, 1265 (2004) http://dx.doi.org/10.1007/s00706-004-0206-6[Crossref]
  • [22] X. L. Feng, C. J. Guan and C. X. Zhao, Synth. Commun. 34, 487 (2004) http://dx.doi.org/10.1081/SCC-120027288[Crossref]
  • [23] (a) S. J. Ji, M. F. Zhou, D. G. Gu, S. Y. Wang and T. P. Loh, Synlett 2077 (2003); (b) S. J. Ji, M. F. Zhou, D. G. Gu, Z. Q. Jiang and T. P. Loh, Eur. J. Org. Chem. 1584 (2004) [Crossref]
  • [24] R. R. Nagawade and D. B. Shinde, Acta Chim. Slov. 53, 210 (2006)
  • [25] R. R. Nagawade, D. B. Shinde, Bull. Korean Chem. Soc. 26, 12 (2005)
  • [26] A. Srinivasa, P.P. Varma, V. Hulikal and K. M. Mahadevan, Monatsh. Chem., 39, 111 (2008) http://dx.doi.org/10.1007/s00706-007-0697-z[Crossref]
  • [27] A. Khallafi-Nezhad et. al., Synthesis 617 (2008)
  • [28] H. Firouzabadi, N. Iranpoor, M. Jafarpour, A. Ghaderi, J. Mol. Catal. A: Chem., 253, 249 (2006) http://dx.doi.org/10.1016/j.molcata.2006.03.043[Crossref]
Document Type
Publication order reference
Identifiers
YADDA identifier
bwmeta1.element.-psjd-doi-10_2478_s11532-008-0069-5
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