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Novel catalytic method synthesis of calix[4]pyrroles using Preyssler and Wells-Dawson heteropolyacids Cover

Novel catalytic method synthesis of calix[4]pyrroles using Preyssler and Wells-Dawson heteropolyacids

Green Sciences
Volume 13 (2011): Issue 2 (June 2011)
By: ,   and    
Open Access
|Jun 2011
References

References

  1. Kozhevnikov, I.V. (1998). Catalysis by Heteropoly Acids and Multicomponent Polyoxometalates in Liquid-Phase Reactions.98, 171-198. DOI: 10.1021/cr960400y.
    Open DOISearch in Google Scholar
  2. Izumi, Y., Urabe, K. & Onaka, M. (1992). Zeolite, Clay and Heteropoly Acid in Organic Reactions, Kodansha/VCH, Tokyo.
    Search in Google Scholar
  3. Okuhara, T., Mizuno., N. & Misono, M. (1996).. 41, 113-252.
    Search in Google Scholar
  4. Gale, P.A., Sessler, J.L. & Král, V. (1998). Calixpyrroles.1-8. DOI: 10.1039/A706280J.
    Open DOISearch in Google Scholar
  5. Chupakhin, O.N., Rusinov, G.L., Itsikson, N.A., Beresnev, D.N. & Kodess, M.I. (2003)., Lisbon. p. 2.01.
    Search in Google Scholar
  6. Chauhan, S.M.S., Sahoo, B.B. & Sriniwas, K.A. (2001). Microwave assisted synthesis of 5,10,15,20-tetraarylporphyrins.31, 33-37. DOI: 10.1081/SCC-100000176.
    Open DOISearch in Google Scholar
  7. Geier, G.R., Haynes, D.M. & Lindsey, J.S. (1999). An efficient one-flask synthesis of-confused tetraphenylporphyrin.1455-1458. DOI: 10.1021/ol9910114.
    Open DOISearch in Google Scholar
  8. Chandrashekar, T.K. & Venkatraman, S. (2003). Core-modified expanded porphyrins: new generation organic materials.36, 676-691. DOI: 10.1021/ar020284n.
    Open DOISearch in Google Scholar
  9. Rothenmund, P. & Gage, V. (1955). Concerning the structure of acetonepyrrole.77, 3340-3341. DOI: 10.1021/ja00117a004.
    Open DOISearch in Google Scholar
  10. Sessler, J.L., Camiolo, S. & Gale, P.A. (2003). Pyrrolic and polypyrrolic anion binding agents.240, 17-55. DOI: 10.1016/S0010-8545(03)00023-7.
    Open DOISearch in Google Scholar
  11. Gale, P.A., Sessler, J.L., Král, V. & Lynch, V.J. (1996). Calix[4]pyrroles: Old yet new anion-binding agents.118, 5140-5141. DOI: 10.1021/ja960307r.
    Open DOISearch in Google Scholar
  12. Bachmann, J. & Nocera, D.G. (2005). Multielectron redox chemistry of iron porphyrinogens. J. Am. Chem. Soc. 127, 4730-4743. DOI: 10.1021/ja043132r.
    Open DOISearch in Google Scholar
  13. Miyaji, H., Anzenbacher, P., Sessler, J.L., Bleasdale, E.R. & Gale, P.A. (1999). Anthracene-linked calix[4]pyrroles: fluorescent chemosensors for anions.1723-1724. DOI: 10.1039/A905054J.
    Open DOISearch in Google Scholar
  14. Gale, P.A., Twyman, L.J., Handlin, C.I., Sessler, J.L. (1999). A colourimetric calix[4]pyrrole-4-nitrophenolate based anion sensor.1851-1852. DOI: 10.1039/A905743I.
    Open DOISearch in Google Scholar
  15. Gale, P.A., Hursthouse, M.B., Light, M.E., Sessler, J.L., Warriner, C.N. & Zimmerman, R.S. (2001). Ferrocene-substituted calix[4]pyrrole: a new electrochemical sensor for anions involving CH anion hydrogen bonds.42, 6759-6762. DOI: 10.1016/S0040-4039(01)01337-5.
    Open DOISearch in Google Scholar
  16. Král, V., Gale, P.A., Anzenbacher, Jr. P., Jursíková, K., Lynch, V. & Sessler, J.L. (1998). Calix[4]pyridine: a new arrival in the heterocalixarene family.9-10. DOI: 10.1039/A706018A.
    Open DOISearch in Google Scholar
  17. Conoci, S., Palumbo, M., Pignataro, B., Rella, R., Valli, L. & Vasapollo, G. (2002). Optical recognition of organic vapors through ultra thin calix[4]pyrrole films.198, 869-873. DOI: 10.1016/S0927-7757(01)01013-5.
    Open DOISearch in Google Scholar
  18. Floriani, C. (1996). The porphyrinogen-porphyrin relationship: the discovery of artificial porphyrins.1257-1263. DOI: 10.1039/CC9960001257.
    Open DOISearch in Google Scholar
  19. Depraetere, S., Smet, M. & Dehaen, W. (1999).-confused calix[4]pyrroles.38, 3359-3361. DOI: 10.1002/(SICI)1521-3773(19991115)38:22<3359::AID-ANIE3359>3.0.CO;2-K.
    Open DOISearch in Google Scholar
  20. Anzenbacher, Jr. P., Jursíková, K., Lynch, V.M., Gale, P.A. & Sessler, J.L. (1999). Calix[4]pyrroles containing deep cavities and fixed walls. Synthesis, structural studies, and anion binding properties of the isomeric products derived from the condensation of p-hydroxyacetophenone and Pyrrole.121, 11020-11021. DOI: 10.1021/ja993195n.
    Open DOISearch in Google Scholar
  21. Miyaji, H., Hong, S., Jeong, D., Yoon, D., Na, H., Hong, J., Ham, S., Sesseler, J.L. & Lee, C.A. (2007). A Binol-Strapped Calix[4]pyrrole as a Model Chirogenic Receptor for the Enantioselective Recognition of Carboxylate Anions.46, 2508-2511. DOI: 10.1002/anie.200604161.
    Open DOISearch in Google Scholar
  22. Radha Kishan, M., Srinivas, N., Raghavan, K.V., Kulkarni, S.J. & Sarma, J.A.R.P. (2001). A novel, shape-selective, zeolite-catalyzed synthesis of calix[4]pyrroles.2226-2227. DOI: 10.1039/B105690P.
    Open DOISearch in Google Scholar
  23. Bamoharram, F.F., Heravi, M.M., Roshani, M., Jahangir, M. & Gharib, A. (2006). Preyssler catalyst, [NaPWO]: A green, efficient and reusable catalyst for esterification of salicylic acid with aliphatic and benzylic alcohols.302, 42-47. DOI: 10.1016/j.apcata.2005.12.021.
    Open DOISearch in Google Scholar
  24. Romanelli, G., Autino, J.C., Baronetti, G. & Thomas, H. (2001). H. Efficient Deprotection of Phenol Methoxymethyl Ethers Using a Solid Acid Catalyst with Wells-Dawson Structure.6, 1006-1011. DOI: 10.3390/61201006.
    Open DOISearch in Google Scholar
  25. Anzenbacher, Jr. P., Nishibayu, R. & Palacios, M.A. (2006).-confused calix[4]pyrrole.250, 2929-2938. DOI: 10.1016/j.ccr.2006.09.001.
    Open DOISearch in Google Scholar
DOI: https://doi.org/10.2478/v10026-011-0027-4 | Journal eISSN: 3072-0389 (formerly 1899-4741) | Journal ISSN: 1509-8117
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Language: English
Page range: 70 - 73
Published on: Jun 16, 2011
Published by: West Pomeranian University of Technology, Szczecin
In partnership with: Paradigm Publishing Services
Publication frequency: Volume open
Keywords:
Calix[4]pyrrole,
Heteropolyacid,
Preyssler,
Wells-Dawson,
Catalysis,
N-confused calix[4]pyrrole
Related subjects:
Industrial chemistry,
Biotechnology,
Chemical engineering,
Process engineering

© 2011 Ali Gharib, Manouchehr Jahangir, J. Scheeren, published by West Pomeranian University of Technology, Szczecin
This work is licensed under the Creative Commons License.

Volume 13 (2011): Issue 2 (June 2011)
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