Full-text resources of PSJD and other databases are now available in the new Library of Science.
Visit https://bibliotekanauki.pl

PL EN


Preferences help
enabled [disable] Abstract
Number of results

Journal

2010 | 8 | 3 | 669-673

Article title

Efficient Lewis acid-assisted Brønsted acid (LBA) catalysis in the iron-catalyzed Friedel-Crafts alkylation reaction of indoles

Content

Title variants

Languages of publication

EN

Abstracts

EN
Lewis acid-assisted Brønsted acid (LBA) catalysis was proposed for the iron-catalyzed Friedel-Crafts alkylation of indoles with chalcones. This proposal was supported by the ESI-MS and cyclic voltammetry. The addition of acac to the iron-catalyzed Friedel-Crafts alkylation of indoles with chalcones created a powerful catalytic system, which makes the alkylation reactions occur easily under mild conditions. [...]

Publisher

Journal

Year

Volume

8

Issue

3

Pages

669-673

Physical description

Dates

published
1 - 6 - 2010
online
25 - 4 - 2010

Contributors

author
  • Key Laboratory of Organosilicon Chemistry and Material Technology of Ministry of Education, Hangzhou Normal University, Hangzhou, 310012, P. R. China
author
  • Key Laboratory of Organosilicon Chemistry and Material Technology of Ministry of Education, Hangzhou Normal University, Hangzhou, 310012, P. R. China
author
author
  • Key Laboratory of Organosilicon Chemistry and Material Technology of Ministry of Education, Hangzhou Normal University, Hangzhou, 310012, P. R. China
author
  • Key Laboratory of Organosilicon Chemistry and Material Technology of Ministry of Education, Hangzhou Normal University, Hangzhou, 310012, P. R. China
  • Key Laboratory of Organosilicon Chemistry and Material Technology of Ministry of Education, Hangzhou Normal University, Hangzhou, 310012, P. R. China
author
  • Department of Chemistry, National University of Singapore, Singapore, 117543, Republic of Singapore
author
  • Key Laboratory of Organosilicon Chemistry and Material Technology of Ministry of Education, Hangzhou Normal University, Hangzhou, 310012, P. R. China

References

  • [1] W.J. Houlihan, Indoles; Vol. I (John Wiley & Sons Inc, New York, 1972) 71
  • [2] S.W. Remiszewski et al., J. Med. Chem. 46, 4609 (2003) http://dx.doi.org/10.1021/jm030235w[Crossref]
  • [3] M. Ishikura, K. Yamada, Nat. Prod. Rep. 26, 803 (2009) http://dx.doi.org/10.1039/b820693g[Crossref]
  • [4] M.A. Metwally, S. Shaaban, B.F. Abdel-Wahab, G.A. El-Hiti, Curr. Org. Chem. 13, 1475 (2009) http://dx.doi.org/10.2174/138527209789055063[Crossref]
  • [5] A. Zicmanis, G. Vavilina, S. Drozdova, P. Mekss, M. Klavins, Central Eur. J. Chem. 5, 156 (2007) http://dx.doi.org/10.2478/s11532-006-0063-8[Crossref]
  • [6] M. Bandini, A. Eichholzer, Amgew. Chem. Int. Ed. 48, 9608 (2009) [Crossref]
  • [7] R. Jiang, X.P. Xu, T. Chen, H.Y. Li, G. Chen, S.J. Ji, Synlett 2815 (2009)
  • [8] K. Akagawa, T. Yamashita, S. Sakamoto, K. Kudo, Tetrahedron Lett. 50, 5602 (2009) http://dx.doi.org/10.1016/j.tetlet.2009.07.071[Crossref]
  • [9] H.M. Meshram, D.A. Kumar, B.C. Reddy, Helv. Chim. Acta 92, 1002 (2009) http://dx.doi.org/10.1002/hlca.200800410[Crossref]
  • [10] M. Bandini, P.G. Cozzi, M. Giacomini, P. Melchiorre, S. Selva, A. Umani-Ronchi, J. Org. Chem. 67, 3700 (2002) http://dx.doi.org/10.1021/jo0163243[Crossref]
  • [11] G. Bartoli, M. Bosco, A. Carlone, F. Pesciaioli, L. Sambri, P. Melchiorre, Org. Lett. 9, 1403 (2007) http://dx.doi.org/10.1021/ol070309o[Crossref]
  • [12] M. Agnusdel, M. Bandini, A. Melloni, A. Umani-Ronchi, J. Org. Chem. 68, 7126 (2003) http://dx.doi.org/10.1021/jo034466m[Crossref]
  • [13] H. Firouzabadi, N. Iranpoor, F. Nowrouzi, Chem. Commun. 789 (2005) [Crossref]
  • [14] D.P. Li, Y.C. Guo, Y. Ding, J.C. Xiao, Chem. Commun. 799 (2006) [Crossref]
  • [15] J.S. Yadav, B.V.S. Reddy, G.. Narasimhulu, G. Satheesh, Synlett 727 (2009) [Crossref]
  • [16] C. Bolm, J. Legros, J.L. Paih, L. Zani, Chem. Rev. 104, 6217 (2004) http://dx.doi.org/10.1021/cr040664h[Crossref]
  • [17] A.A.O. Sarhan, C. Bolm, Chem. Soc. Rev. 38, 2730 (2009) http://dx.doi.org/10.1039/b906026j[Crossref]
  • [18] M.S. Yang, L.W. Xu, F.B. Zhang, H.Y. Qiu, J.X. Jiang, G.Q. Lai, Appl. Organomet. Chem. 22, 177 (2008) http://dx.doi.org/10.1002/aoc.1368[Crossref]
  • [19] A.V. Reddy, K. Ravinder, T.V. Goud, P. Krishnaiah, T.V. Raju, Y. Venkateswarlu, Tetrahedron Lett. 44, 6257 (2003) http://dx.doi.org/10.1016/S0040-4039(03)01555-7[Crossref]
  • [20] W. Zhou, L.W. Xu, L. Yang, P.Q. Zhao, C.G. Xia, J. Mol. Catal. A: Chem. 249, 129 (2006) http://dx.doi.org/10.1016/j.molcata.2006.01.005[Crossref]
  • [21] H. Yamamoto, K. Futatsugi, Angew. Chem. Int. Ed. 44, 1924 (2005) http://dx.doi.org/10.1002/anie.200460394[Crossref]
  • [22] H. Yamamoto, Tetrahedron 63, 8377 (2007) http://dx.doi.org/10.1016/j.tet.2007.05.128[Crossref]
  • [23] J. Heinze, Angew. Chem. Int. Ed. 23, 831 (1984) http://dx.doi.org/10.1002/anie.198408313[Crossref]
  • [24] P.L. Boulas, M. Gómez-Kaifer, L. Echegoyen, Angew. Chem. Int. Ed. 37, 216 (1998) http://dx.doi.org/10.1002/(SICI)1521-3773(19980216)37:3<216::AID-ANIE216>3.0.CO;2-P[Crossref]
  • [25] K. Daasbjerg, H. Svith, S. Grimme, M. Gerenkamp, C. Muck-Lichtenfeld, A. Barchuk, F. Keller, Angew. Chem. Int. Ed. 45, 2041 (2006) http://dx.doi.org/10.1002/anie.200504176[Crossref]

Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.-psjd-doi-10_2478_s11532-010-0016-0
JavaScript is turned off in your web browser. Turn it on to take full advantage of this site, then refresh the page.