Niobium(V) chloride: An efficient catalyst for selective acetylation of alcohols and phenols

Journal of Molecular Catalysis A: Chemical

Volumn 230, Issue 1-2, 2005, Pages 107-111

  Yadav, J S ^a   Narsaiah, A V ^a   Reddy, B V S ^a   Basak, A K ^a   Nagaiah, K ^a  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

Acetylation; Alcohols; Methylenedichloride; Niobium(V) chloride

Indexed keywords

ACETYLATION; ALCOHOLS; CATALYSTS; THERMAL EFFECTS;

ACETIC ANHYDRIDE; NIOBIUM (V) CHLORIDE; ROOM TEMPERATURE;

NIOBIUM COMPOUNDS;

ACETIC ANHYDRIDE; ALCOHOL DERIVATIVE; FUNCTIONAL GROUP; NIOBIUM; PHENOL DERIVATIVE;

ACETYLATION; ARTICLE; CATALYST; CHEMICAL PROCEDURES; CHEMICAL REACTION; REACTION ANALYSIS; ROOM TEMPERATURE;

EID: 14644443545     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2004.12.012     Document Type: Article

References (32)

1. P. Arya, D.T.H. Chou, and M.G. Back Angew. Chem., Int. Ed. 40 2000 339
2. R.I. Zhdanov, and S.M. Zhendarova Synthesis 1975 222
3. G. Hofle, V. Steglich, and H. Vorbruggen Angew. Chem., Int. Ed. 17 1978 569
4. E.F.V. Scrieven Chem. Soc. Rev. 12 1983 129
5. T. Hirose, B.G. Kopek, Z.H. Wang, R. Yusa, and B.W. Baldwin Tetrahedron Lett. 2003 1831
6. S. Paul, P. Nanda, R. Gupta, and A. Loupy Tetrahedron Lett. 43 2002 4261
7. E. Vedejs, and S.T. Diver J. Am. Chem. Soc. 115 1993 3358
8. J. Iqbal, and R.R. Srivastava J. Org. Chem. 57 1992 2001
9. S. Chandrasekhar, T. Ramachander, and M. Takhi Tetrahedron Lett. 39 1998 3263
10. K.D. Surya Tetrahedron Lett. 45 2004 2919
11. P. Prodeep Tetrahedron Lett. 45 2004 4785
12. E.W.P. Damen, L. Braamer, and H.W. Scheeren Tetrahedron Lett. 39 1998 6081
13. A.-X. Li, T.-S. Li, and T.-H. Ding Chem. Commun. 1997 1389
14. P.M. Bhaskar, and D. Loganadhan Tetrahedron Lett. 39 1998 2215
15. V.K. Yadav, K.G. Babu, and M. Mittal Tetrahedron 57 2001 7047
16. E. Vedejs, and O. Daugulis J. Org. Chem. 61 1996 5702
17. B.A. D'Sa, and J.G. Verkade J. Org. Chem. 61 1996 2963
18. K. Ishihara, M. Kubota, H. Kurihara, and H. Yamamoto J. Am. Chem. Soc. 117 1995 4413
19. P. Saravanan, and V.K. Singh Tetrahedron Lett. 40 1999 2611
20. T. Mukaitama, I. Shiina, and M. Miyashita Chem. Lett. 1992 625
21. K.L. Chandral, P. Saravanan, K.S. Rajesh, and V.K. Singh Tetrahedron 2002 1369
22. K. Ishihara, M. Kubota, and H. Yamamot Synlett 1996 265
23. M. Miyashita, I. Shiina, S. Miyoshi, and T. Mukaiyama Bull. Chem. Soc. Jpn. 66 1993 1516
24. P. Allevi, P. Ciuffreda, A. Longa, and M. Anastasia Tetrahedron Asymm. 9 1998 2915
25. R. Ballini, G. Bosica, S. Carloni, L. Ciaralli, R. Maggi, and G. Sartori Tetrahedron Lett. 39 1998 6049
26. J.S. Yadav, B.V.S. Reddy, A.K. Basak, and A.V. Narsaiah Tetrahedron Lett. 44 2003 2217
27. J.S. Yadav, B.V.S. Reddy, A.K. Basak, and A.V. Narsaiah Green Chem. 5 2003 3
28. J.S. Yadav, B.V.S. Reddy, A.K. Basak, B. Vishali, A.V. Narsaiah, and K. Nagaiah Eur. J. Org. Chem. 2004 546
29. A.V. Narsaiah, and K. Nagaiah Synthesis 2003 1881
30. A.V. Narsaiah, and K. Nagaiah Synthesis 2004 1253
31. A.V. Narsaiah, and K. Nagaiah Synth. Commun. 21 2003 3825
32. A.V. Narsaiah, and K. Nagaiah Ind. J. Chem., Sec. B 42 2003 2045