DOI QR코드

DOI QR Code

Caffeinilium Chlorochromate: As a Mild and Efficient Reagent for Oxidation of Alcohols and Chemoselective Oxidative Cleavage of Oximes

  • Shirini, F. (Department of Chemistry, College of Science, Guilan University) ;
  • Mohammadpoor Baltork, I. (Department of Chemistry, College of Science, Isfahan University) ;
  • Hejazi, Z. (Department of Chemistry, College of Science, Guilan University) ;
  • Heravi, P. (Department of Chemistry, College of Science, Guilan University)
  • Published : 2003.04.20

Abstract

Keywords

References

  1. Cainelli, G.; Cardillo, G. Chromium Oxidations in Organic Chemistry; Springer-Verlag: Berlin, 1984; Vol 19.
  2. Luzzio, F. A.; Guziec, F. S. Org. Prep. & Procedure Int. 1988, 20, 533. https://doi.org/10.1080/00304948809356301
  3. Firouzabadi, H.; Sharifi, A. Synthesis 1992, 999.
  4. Li, M.; Johnson, M. E. Synth. Commun. 1995, 25, 533. https://doi.org/10.1080/00397919508011387
  5. Lee, J. G.; Lim, H. J.; Ha, D. S. Bull. Korean Chem. Soc. 1987, 8, 435.
  6. Salehi, P.; Khodaei, M. M.; Goodarzi, M. Synth. Commun. 2002, 32, 1259. https://doi.org/10.1081/SCC-120003618
  7. Khodaei, M. M.; Salehi, P.; Goodarzi, M. Synth. Commun. 2001, 31, 1253. https://doi.org/10.1081/SCC-100104013
  8. Zhang, G.-S.; Chai, B. Indian J. Chem., Sec. B; Org. Chem. Med. Chem. 2001, 40(12), 1264.
  9. Tajbakhsh, M.; Ghaemi, M.; Sarabi, S.; Ghasemzadeh, M.; Heravi, M. M. Monatshefte Fure Chemie 2000, 131, 1213. https://doi.org/10.1007/s007060070030
  10. Shirini, F.; Tajik, H.; Jalili, F. Synth. Commun. 2001, 31, 2885. https://doi.org/10.1081/SCC-100105658
  11. Shirini, F.; Azadbar, M. R. Synth. Commun. 2001, 31, 3775. https://doi.org/10.1081/SCC-100108227
  12. Shirini, F.; Zolfigol, M. A.; Pourhabib, A. J. Chem. Res.(S) 2001, 476.
  13. Shirini, F.; Zolfigol, M. A.; Mallakpour, B.; Mallakpour, S. E.; Hajipour, A. R. Australin J. Chem. 2001, 54, 405. https://doi.org/10.1071/CH01104
  14. Shirini, F.; Mamaghani, M.; Parsa, F.; Mohammadpour-Baltork, I. Bull. Korean Chem. Soc. 2002, 23, 1683. https://doi.org/10.5012/bkcs.2002.23.11.1683

Cited by

  1. α-Naphthyltriphenylphosphonium Peroxodisulfate: A Selective and Regenerable Reagent for Oxidation of Organic Compounds vol.183, pp.6, 2008, https://doi.org/10.1080/10426500701648051
  2. Fast selective oxidation of alcohols under solvent-free conditions vol.39, pp.7, 2013, https://doi.org/10.1007/s11164-012-0846-9
  3. Copper(II) nanoparticles: an efficient and reusable catalyst in green oxidation of benzyl alcohols to benzaldehydes in water vol.30, pp.10, 2016, https://doi.org/10.1002/aoc.3509
  4. A novel lipopathic Cr(VI) oxidant for organic substrates: Kinetic study of oxidation of benzyl alcohol vol.38, pp.11, 2006, https://doi.org/10.1002/kin.20198
  5. Some aspects of tetramethylammonium fluorochromate (VI) oxidations and identification of the reduced chromium species vol.32, pp.4, 2007, https://doi.org/10.1007/s11243-007-0185-7
  6. Caffeinilium Chlorochromate: As a Mild and Efficient Reagent for Oxidation of Alcohols and Chemoselective Oxidative Cleavage of Oximes. vol.34, pp.35, 2003, https://doi.org/10.1002/chin.200335029
  7. HEXAMETHYL ENETETR AMMONIUM FLUOROCHROMATE. A NEW REAGENT FOR OXIDATION OF ORGANIC SUBSTRATES vol.36, pp.4, 2004, https://doi.org/10.1080/00304940409458680
  8. Tripropylammonium Fluorochromate (TriPAFC): A Convenient New Reagent for Oxidation of Organic Substrates vol.25, pp.8, 2003, https://doi.org/10.5012/bkcs.2004.25.8.1277
  9. Oxidation of Alcohol by Lipopathic Cr(VI): A Mechanistic Study vol.71, pp.18, 2003, https://doi.org/10.1021/jo0608772
  10. Oxidation of Organic Substrates Using Two Triethylammonium Halochromates(VI), (C2H5)3NH[CrO3X], (X=F, Cl) Supported on Silica Gel vol.55, pp.1, 2003, https://doi.org/10.1002/jccs.200800034
  11. Crystal structure and solid state computational (DFT/Hirshfeld surface) study for probing a new efficient and recyclable oxidation reagent, 1,2-ethandiylbis(triphenylphosphonium) peroxodisulfate dihyd vol.191, pp.10, 2003, https://doi.org/10.1080/10426507.2016.1206106
  12. Dabco Ammonium Halochromates, $$ {\text{C}}_{6} {\text{H}}_{14} {\text{N}}_{2}\,^{ + } $$ C 6 H 14 N 2 + $$ {\text{Cr}}_{2} {\text{F}}_{2} {\text{O}}_{6}\,^{ - } $$ Cr 2 F 2 O 6 - (DAXC, X = F, Cl), R vol.42, pp.3, 2003, https://doi.org/10.1007/s40995-018-0497-9