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Number of results
2012 | 1 | 6-9

Article title

Amberlyst-15 catalyzed acetylation of phenols and alcohols under solvent free conditions

Content

Title variants

Languages of publication

EN

Abstracts

EN
Amberlyst-15 has been found to be an efficient reusable heterogeneous catalyst for acetylation of phenols and alcohols under solvent free conditions.

Publisher

Year

Volume

1

Pages

6-9

Physical description

Dates

online
23 - 8 - 2012

Contributors

  • Department of Chemistry, Institute of Chemical Technology, N. M. Parikh Road, Matunga, Mumbai - 400019, India
  • Department of Chemistry, Institute of Chemical Technology, N. M. Parikh Road, Matunga, Mumbai - 400019, India

References

  • A. K. Chakraborti, M. K. Nayak, L.. Sharma, J. Org. Chem. 67, 1776 (2002)
  • T. W. Greene, P. G. M. Greene and Wuts, Protective Groups in Organic Synthesis (3rd edn.), Wiley, New York, (1999)
  • M.A. Malden, Protective Groups in Organic Synthesis (1st edn.), Blackwell Science Inc. (1999)
  • A. K. Chakraborti, M. K. Nayak, L. Sharma, J. Org. Chem. 64, 8027 (1999).
  • T. Sano, K. Ohashi, T.Oriyama, Synthesis 7, 1141 (1999)
  • R. I. Zhdanov, S. M. Zhenodarova, Synthesis 4 , 222 (1977)
  • E. F. V. Scriven, Chem Soc Rev. 12, 129 (1983)
  • E. Vedejs, N. S. Bennett, L. M. Conn, S. T. Diver, M. Gingras, S. Lin, P. A. Oliver, M. J. Peterson, J. Org Chem., 58, 7286 (1993)
  • A. C. Cope, E. C. Herrich, Org. Synth Coll Vol. IV. John Wiley and Sons, Inc., New York. (1963)
  • S. Chandrasakhar, T. Ramachander, M.Takhi, Tetrahedron Lett., 39, 3263 (1998)
  • S. K. De, Tetrahedron Lett., 45, 2919 (2004)
  • M.H. Sarvari, H. Sharghi. Tetrahedron, 61, 10903 (2005)
  • K. Jeyakumar, D. K. Chand, J. Mol. Catal. A: Chem., 255, 275 (2006)
  • T–S. Jin, Y –R. Ma, Z –H. Zhang, T –S. Li, Synth. Commun., 28, 3173 (1998)
  • A.K. Chkraborti, R. Gulhane, Chem Commun., 15, 1896 (2003)
  • F. Shirini, M. A. Zolfigol, K. Mohammadi, Bull Korean Chem Soc., 25, 325 (2004)
  • R. Kumareswaran, K. Pachamuthu, Y. D. Vankar, Synlett., 11, 1652 (2000)
  • R. Ghosh, S. Maiti, A. Chakraborty, Tetrahedron Lett.,46, 147 (2005)
  • A.N. Parvulescu, B. C.Gagea, G. Poneelet, V. I. Parvulescu, Appl. Catal. A. : Gen. 301, 133 (2006)
  • B.C. Ranu, P. Dutta, A. Sarkar, J. Chem. Soc., Perkin Trans. 1. 14, 2223 (2000)
  • M.L. Kantam, Aziz P Khatiza, R. Likhar, Catal. Commun. 7, 484 (2006)
  • G.P. Romanelli, D. O. Bennardi, J. C. Autino, G. T. Baronetti and H. J. Thomas E-Journal of Chemistry 5, 641 (2008)
  • (a) M.A. Harmer, Industrial processes using solid acid catalysts, in Handbook of Green Chemistry and Technology; J. H. Clark, D. J. Macquarris, eds.; Blackwell Publishers London. (2002) (b) S. B. Patil, P. R. Singh, M. P. Surpur, S. D. Samant, Synth. Commun., 37, 1659 (2007) (c) M. P. Surpur, P. R. Singh, S.B. Patil, & S.D. Samant, Synth. Commun., 37, 1965 (2007) (d) M. A. Pande, S. D. Samant, Synth. Commun., 41, 754 (2011) (e) A. Chakrabarti, M. M. Sharma, React. Polym., 20, 1 (1993)
  • A. Shaabani, A. Rahmati, Z. Badri, Catal. Commun., 9, 13 (2008)

Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.-psjd-doi-10_2478_recat-2012-0002
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