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Number of results
2009 | 11 | 3 | 5-7

Article title

Novel catalytic synthesis of 6,7-dimethoxyisatin with the use of heteropolyacids (HPAs) as acid solid catalyst

Content

Title variants

Languages of publication

EN

Abstracts

EN
An efficient method for the preparation of 6,7-dimethoxyisatin and its derivatives was developed with good yield by using Preyssler-type heteropolyacid (HPA) as acid catalyst under green conditions. The comparison between Keggin type heteropolyacids, H3[PW12O40], H4[SiW12O40] and H4[SiMo12O40], H3[PMo12O40] and mineral acids with Preyssler's anion shows that the latter possess better catalytical activity than the other heteropolyacids and no degradation of the structure was observed.

Publisher

Year

Volume

11

Issue

3

Pages

5-7

Physical description

Dates

published
1 - 1 - 2009
online
9 - 10 - 2009

Contributors

author
  • School of Pharmacy, Memorial University of Newfoundland, St. John's, Newfoundland, Canada A1C 3V6
author
  • Cluster for Molecular Chemistry, Department of Organic Chemistry, Radboud University Nijmegen, The Netherlands
  • Department of Chemistry, School of Science, Islamic Azad University, Mashhad, IRAN
author
  • Department of Chemistry, School of Science, Islamic Azad University, Mashhad, IRAN
  • Department of Chemistry, School of Science, Islamic Azad University, Mashhad, IRAN

References

  • 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. Molecules. 6, 1006-1011. DOI:10.3390/61201006.[Crossref]
  • Okuhara, T., Mizuno, N. & Misono, M. (1996). Advances in Catalysis. Catalytic Chemistry of Heteropoly compounds. 41, 113-252.
  • Kozhevnikov, I. V. (1987). Advances in catalysis by heteropoly acids. Advances in catalysis by heteropoly acids. Russ. Chem. Rev. 56(9), 811-825. DOI: 10.1070/RC1987v056n09ABEH003304.[Crossref]
  • Joaquim, F. M., Simon, J. G. & Angelo, C. P. (2001). The Chemistry of Isatins: a Review from 1975 to 1999. J. Braz. Chem. Soc. 12 (3), 273-324. DOI: 10.1590/S0103-50532001000300002.[Crossref]
  • Bergman, J., Lindström, J. O. & Tilstam, U. (1985). The structure and properties of some indolic constituents in Couroupita guianensis aubl. Tetrahedron. 41 (14), 2879-2881. DOI:10.1016/S0040-4020(01)96609-8.[Crossref]
  • Kapadia, G. J., Shukla, Y. N., Basak, S. P., Sokoloski, E. A. & Fales, H. M. (1980). The melosatins a novel class of alkaloids from melochia tomentosa. Tetrahedron. 36, 2441-2447. DOI:10.1016/0040-4020(80)80221-3.[Crossref]
  • Hodges, R. J., Ronaldson, W., Taylor, A. & White, E. P. (1963). Sporidesmins. Part II. The structure of degradation products related to 5-chloro-6,7-dimethoxyisatin. J. Chem. Soc. 5332-5336. DOI: 10.1039/JR9630005332.[Crossref]
  • Gulland, J. M., Robinson, R., Scott, J. & Thornley, S. (1929). 6: 7-Dimethoxyisatin, 5: 6-methylenedioxyisatin, and the nuclear degradation of 3: 4-methylenedioxyquindoline. J. Chem. Soc. 2924-2927. DOI: 10.1039/JR9290002924.[Crossref]
  • Bamoharram, F. F., Heravi, M. M., Roshani, M., Gharib, A. & Jahangir, M. (2006). A catalytic method for synthesis of γ-butyrolactone, ε-caprolactone and 2-cumaranone in the presence of Preyssler's anion, [NaP5W30O110]14-, as a green and reusable catalyst. J. Mol. Catal. 252, 90-95. DOI:10.1016/j.molcata.2006.01.067.[Crossref]

Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.-psjd-doi-10_2478_v10026-009-0028-8
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