Ni/Silica catalyzed acetylation of phenols and naphthols: An eco-friendly approach

Arabian Journal of Chemistry

Volumn 7, Issue 1, 2014, Pages 53-56

  Alam, Manawwer ^a   Rahman, Ateeq ^b   Alandis, Naser M ^a   Shaik, Mohammed Rafi ^a  

^a KING SAUD UNIVERSITY   (Saudi Arabia)

^b Vidya Vikas College of Engineering Chevella   (India)

Author keywords

Acetic anhydride; Acetylation; Catalyst; Naphthol; Ni SiO2; Phenol

Indexed keywords

4-CYCLE; ACETIC ANHYDRIDES; AROMATIC ESTERS; ECO-FRIENDLY; LIQUID PHASE CONDITIONS; SUBSTITUTED PHENOL;

ACETYLATION; CATALYSTS; ENVIRONMENTAL PROTECTION; ESTERIFICATION; ESTERS; NAPHTHOL; PHENOLS; REUSABILITY;

CATALYST SELECTIVITY;

EID: 84891373264     PISSN: 18785352     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.arabjc.2012.12.011     Document Type: Article

References (34)

1. Bartoli G., Bosco M., Dalpozzo R., Marcantoni E., Massaccesi M., Sambri L. Eur. J. Org. Chem. 2003, 2003:4611-4617.
2. Bartoli G., Dalpozzo R., Nino A.D., Maiuolo L., Nardi M., Procopio A., Tagarelli A. Green Chem. 2004, 6:191-192.
3. Bodanszky M. Peptide Chemistry 1993, Springer, Berlin.
4. Chakraborti A.K., Gulhane R. Synlett 2004, 2004:627-630.
5. Chakraborti A.K., Gulhane R. Tetrahedron Lett. 2003, 44:6749-6753.
6. Chakraborti A.K., Shivani R. J. Org. Chem. 2006, 71:5785-5788.
7. Chakraborti A.K., Gulhane R. Chem. Commun. 2003, 1896-1897.
8. Chakraborti A.K., Gulhane R. Tetrahedron Lett. 2003, 44:3521-3525.
9. Chakraborti A.K., Gulhane R., Shivani R. Synlett 2003, 203:1805-1808.
10. Chakraborti A.K., Gulhane R., Shivani R. Synthesis 2004, 111-115.
11. Chakraborti A.K., Sharma L., Gulhane R., Shivani R. Tetrahedron 2003, 59:7661-7668.
12. Chen C.T., Kuo J.H., Pawar V.D., Munot Y.S., Weng S.S., Ku C.H., Liu C.Y. J. Org. Chem. 2005, 70:1188-1197.
13. Crouse D.J., Hulbut S.L., Wheeler D.M.S. J. Org. Chem. 1981, 46:374-378.
14. Dalpozzo R., Nino A.D., Maiuolo L., Oliverio M., Procopio A., Russo B., Tocci A. Aust. J. Chem. 2007, 60:75-79.
15. De S.K. Tetrahedron Lett. 2004, 45:2919-2922.
16. Firouzabadi H., Iranpoor N., Farahi S. J. Mol. Catal. A 2008, 289:61-68.
17. Greene T.W., Wuts P.G.M. Protective Groups in Organic Synthesis 1991, John Wiley & Sons Inc., New York.
18. Ghosh R., Maiti S., Chakraborty A. Tetrahedron Lett. 2005, 45:147-151.
19. Ishihara K., Kubota M., Yamamoto H. Synlett 1996, 1996:265-266.
20. Ishihara K., Kubota M., Kurihara H., Yamamoto H. J. Org. Chem. 1996, 61:4560-4567.
21. Kamal A., Khan M.N.A., Reddy K.S., Srikanth Y.V.V., Krishnaji T. Tetrahedron Lett. 2007, 48:3813-3818.
22. Magrath J., Abeles R.H. J. Med. Chem. 1992, 35:4279-4283.
23. Miyashita M., Shina I., Miyoshi S., Mukaiyama T. Bull. Chem. Soc. Jpn. 1993, 66:1516-1527.
24. Moghadam M., Tangestaninejad S., Mirkhani V., Mohammadpour-Baltork I., Shaibani R. J. Mol. Catal. A 2004, 219:73-78.
25. In the Chemistry of Acid Derivatives: Supplement B, Part 1 1979, Interscience, Chichester, pp. 267-490. M.A. Ogliaruso, J.F. Wolfe, S. Patai (Eds.).
26. Procopio A., Dalpozzo R., Nino A.D., Maiuolo L., Russo B., Sindona G. Adv. Synth. Catal. 2004, 346:1465-1470.
27. Procopiou P.A., Baugh S.P.D., Flack S.S., Inglis G.G.A. J. Org. Chem. 1998, 63:2342-2347.
28. Rahman A., Jonnalagadda S.B. Cat. Lett. 2008, 123:264-268.
29. Rahman A., Jonnalagadda S.B. J. Mol. Cat. A 2009, 299:98-101.
30. Rahman A., Pullabhotla V.S.R.R., Jonnalagadda S.B. Cat. Commun. 2008, 9:2417-2421.
31. Roux C.L., Dubac J. Organometallics 1996, 15:4646-4648.
32. Simmonds R.J. Chemistry of Biomolecules: An Introduction 1992, The Royal Society of Chemistry, Cambridge.
33. Shivani R., Gulhane R., Chakraborti A.K. J. Mol. Catal. A 2007, 264:208-213.
34. Tai C.A., Kulkarni S.S., Hung S.C. J. Org. Chem. 2003, 68:8719-8722.