Polystyrene-supported GaCl 3: A new, highly efficient and recyclable heterogeneous Lewis acid catalyst for acetylation and benzoylation of alcohols and phenols

Comptes Rendus Chimie

Volumn 15, Issue 11-12, 2012, Pages 1048-1054

  Rahmatpour, Ali ^a  

^a RESEARCH INSTITUTE OF PETROLEUM INDUSTRY RIPI   (Iran)

Author keywords

Acetylation; Alcohol; Heterogeneous Lewis acid catalyst; Phenol; Polymer supported catalyst

Indexed keywords

EID: 84870238892     PISSN: 16310748     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.crci.2012.08.005     Document Type: Article

References (56)

1. H. Yamamoto Lewis Acids in Organic Synthesis 2002 Wiley-VCH Weinheim
2. S.V. Ley, I.R. Baxendale, R.N. Bream, P.S. Jackson, A.G. Leach, D.A. Longbottom, M. Nesi, J.S. Scott, R.I. Storer, and S.J. Taylor J. Chem. Soc. Perkin Trans. 1 23 2000 3815
3. D.C. Bailey, and S.H. Langer Chem. Rev. 81 1981 109
4. A. Akela, and A. Moet Functionalized Polymers and Their Applications 1990 Wiley New York p. 11
5. N.E. Leadbeater, and M. Marco Chem. Rev. 102 2002 3217
6. A. Akela Chem. Rev. 81 1981 557
7. J.H. Clarck Catalysis of Organic reactions by Supported Inorganic Reagents 1994 VCH Weinheim p. 126
8. K. Smith Solid Supports and Catalysts in Organic Synthesis 1992 Ellis Horwood Chichester
9. R. Ruicheng, J. Shuojian, and S. Ji J. Macromol. Sci. Chem. A. 24 6 1987 669
10. T.W. Greene, and P.G.M. Wuts Protective Groups in Organic Synthesis 3rd ed 2000 John Wiley & Sons New York
11. G. Hofle, W. Steglich, and H. Vorbruggen Angew. Chem. Int. Ed. 17 1978 569
12. E. Vedejs, N.S. Bennett, L.M. Conn, S.T. Diver, M. Gingras, S. Lin, P.A. Oliver, and M.J. Peterson J. Org. Chem. 56 1993 7286
13. A.C. Cope, and E.C. Herrich Organic synthesis collective IV 1963 Wiley New York 304
14. J. Iqbal, and R.R. Srivastava J. Org. Chem. 57 1992 2001
15. G.W. Breton, M.J. Kurtz, and S.L. Kurtz Tetrahedron Lett. 38 1997 3825
16. H. Hagiwara, K. Morohashi, T. Suzuki, M. Ando, I. Yamamoto, and M. Kato Synth. Commun. 28 1998 2001
17. R. Ballini, G. Bosica, S. Carloni, L. Ciaralli, R. Maggi, and G. Sartori Tetrahedron Lett. 39 1998 6049
18. S.V. Pansar, M.G. Malusare, and A.N. Rai Synth. Commun. 30 2000 2587
19. I. Mohammadpoor-Baltork, H. Aliyan, and A.R. Khosropour Tetrahedron 57 2001 5851
20. S. Chandrasekhar, T.S. Tin, Y.R. Ma, Z.H. Zhang, and T.S. Li Synth. Commun. 28 1998 3173
21. T. Ramachander, and M. Takhi Tetrahedron Lett. 39 1998 3263
22. T.S. Tin, Y.R. Ma, Z.H. Zhang, and T.S. Li Synth. Commun. 28 1998 3173
23. T. Srikanth Reddy, M. Narasimhulu, N. Suryakiran, K. Chinni Mahesh, K. Ashalatha, and y. Venkateswarlu Tetrahedron Lett. 255 2006 78
24. R.H. Tale, and R.N. Adude Tetrahedron Lett. 47 2006 7263
25. P.A. Procopiou, S.P.D. Baugh, S.S. Flack, and G.G.A. Inglis J. Org. Chem. 63 1998 2342
26. R. Qiu, G. Zhang, X. Ren, X. Xu, R. Yang, S. Luo, and S. Yin J. Organomet. Chem. 695 2010 1182
27. M.L. Kantam, K. Aziz, and P.R. Likhar Catal. Commun. 7 2006 484
28. R. Ghosh, S. Maiti, and A. Chakraborty Tetrahedron Lett. 46 2005 147
29. A.K. Chakraborti, L. Sharma, A.K. Gulhane, and R. Shivani Tetrahedron 59 2003 7661
30. R. Shivani, A.K. Gulhane, and Chakraborti J. Mol. Catal. A Chem. 264 2007 208
31. A.K. Chakraborti, and R. Gulhane Tetrahedron Lett. 44 2003 3521
32. A.K. Chakraborti, A.K. Gulhane, and R. Shivani Synthesis 2004 111
33. A.K. Chakraborti, and A.K. Gulhane J. Chem. Soc. Chem. Commun. 2003 1896
34. S. Tangestaninejad, M.H. Habibi, V. Mirkhani, and M. Moghadam Synth. Commun. 32 2002 1337
35. M. Moghadam, S. Tangestaninejad, V. Mirkhani, I. Mohammadpoor-Baltork, and R. Shaibani J. Mol. Catal. A Chem. 219 2004 73
36. M. Moghadam, S. Tangestaninejad, V. Mirkhani, I. Mohammadpoor-Baltork, and S.A. Taghavi J. Mol. Catal. A Cjhem. 274 2007 217
37. J.K. Joseph, S.L. Jain, and B. Sain J. Mol. Catal. A Chem. 267 2007 108
38. M. Curini, F. Epifano, M.C. Marcotullio, O. Rosati, and M. Rossi Synth. Commun. 30 2000 1319
39. M. Barbero, S. Cadamuro, S. Dughera, and P. Enturello Synthesis 2008 3625
40. F. Shirini, M.A. Zolfigol, and M. Abedini Monatsh Chem. 140 2009 1495
41. V. Mirkhani, S. Tangestaninejad, M. Moghadam, B. Yadollahi, and L. Alipanah Monatsh Chem. 135 2004 1257
42. A.K. Chakraborti, A.K. Gulhane, and R. Shivani Synlett 2003 1805
43. F. Rajabi Tetrahedron Lett. 50 2009 395
44. B.M. Choudary, M.L. Kantam, B. Bharathi, C. Reddy, and V. Reddy J. Mol. Catal. A Chem. 168 2001 69
45. R. Alleti, M. Perambudura, S. Samantha, and V.P. Reddy J. Mol. Catal. A Chem. 226 2005 57
46. A.K. Chakraborti, and R. Gulhane Tetrahedron Lett. 44 2003 6749
47. A.T. Khan, L.H. Choudhury, and S. Ghosh Eur. J. Org. Chem. 2005 2782
48. M. Salavati-Niasari, S. Hydarzadeh, A. Amiri, and S. Salavati J. Mol. Catal. A Chem. 232 2003 191
49. B. Karimi, and J. Maleki J. Org. Chem. 68 2003 4951
50. A. Rahmatpour Heteroat. Chem. 22 2011 85
51. A. Rahmatpour Heteroat. Chem. 22 2011 51
52. A. Rahmatpour J. Organomet. Chem. 712 2012 15
53. A.P. Deshmukh, K.J. Padiya, and M.M. Salunkhe J. Chem. Res. (S) 9 1999 568
54. I.M. Kolthoff, and E.B. Sandell Textbook of Quantitative In organic Analysis, Macmillan New York 1965
55. D.C. Neckers, D.A. Kooistra, and G.W. Green J. Am. Chem. Soc. 94 1972 9284
56. E.C. Blossey, L.M. Turner, and D.C. Neckers J. Org. Chem. 40 1975 959