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2008 | 6 | 4 | 622-626
Tytuł artykułu

Ionic liquid promoted synthesis of bis(indolyl) methanes

Treść / Zawartość
Warianty tytułu
Języki publikacji
EN
Abstrakty
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. [...]
Wydawca

Czasopismo
Rocznik
Tom
6
Numer
4
Strony
622-626
Opis fizyczny
Daty
wydano
2008-12-01
online
2008-10-28
Twórcy
  • Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad (M.S.), 431004, India
autor
  • Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad (M.S.), 431004, India
  • Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad (M.S.), 431004, India
Bibliografia
  • [1] T. Welton, Chem. Rev. 99, 2071 (1999) http://dx.doi.org/10.1021/cr980032t[Crossref]
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  • [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]
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  • [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]
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  • [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]
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.-psjd-doi-10_2478_s11532-008-0069-5
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