A simple synthetic protocol for oxidation of alkyl-arenes into ketones using a combination of HBr-H2O2

Tetrahedron Letters

Volumn 48, Issue 13, 2007, Pages 2271-2274

  Khan, Abu T ^a   Parvin, Tasneem ^a   Choudhury, Lokman H ^a   Ghosh, Subrata ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY GUWAHATI   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ALKYL GROUP; AROMATIC COMPOUND; BROMIDE; DICHLOROMETHANE; HYDROGEN PEROXIDE; KETONE DERIVATIVE; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE;

ARTICLE; BROMINATION; HYDROLYSIS; NITRATION; OXIDATION; PROTON NUCLEAR MAGNETIC RESONANCE; QUANTUM YIELD; REACTION ANALYSIS; ROOM TEMPERATURE; STEREOCHEMISTRY;

EID: 33847301873     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.01.172     Document Type: Article

References (21)

1. Edwards J.O., and Curci R. In: Strukul G. (Ed). Catalytic Oxidation with Hydrogen Peroxide as Oxidant (1992), Kluwer, Dordrecht 97-151 Chapter 4
2. Warren S. Organic Synthesis: The Disconnection Approach (2004), J. Wiley & Sons, Singapore 57 201 and 330
3. Ghosh S., Banik B.K., and Ghatak U.R. J. Chem. Soc., Perkin Trans. 1 (1991) 3195-3197
4. Compere D., Marazano C., and Das B.C. J. Org. Chem. 64 (1999) 4528-4532
5. Larock R.C. Comprehensive Organic Transformations: A Guide to Functional Group Preparations (1989), VCH, New York p 591
6. Muzart J. Tetrahedron Lett. 28 (1987) 3139-3142
7. Zhao D., and Lee D.G. Synthesis (1994) 915-916
8. Banik B.K., Venkatraman M.S., Mukhopadhyay C., and Becker F.F. Tetrahedron Lett. 39 (1998) 7247-7250
9. Lee N.H., Lee C., and Jung D.S. Tetrahedron Lett. 39 (1998) 1385-1388
10. Kim S.S., Sar S.K., and Tamrakar P. Bull. Korean Chem. Soc. 23 (2002) 937-938
11. Murahashi S.I., Komiya N., Oda Y., Kuwabara T., and Naota T. J. Org. Chem. 65 (2000) 9186-9193
12. Das S., Bhowmick T., Punniyamurthy T., Dey D., Nath J., and Chaudhuri M.K. Tetrahedron Lett. 44 (2003) 4915-4917
13. Valusamy S., and Punniyamurthy T. Tetrahedron Lett. 44 (2003) 8955-8957
14. Nechab M., Einhorn C., and Einhorn J. Chem. Commun. (2004) 1500
15. Bonvin Y., Callens E., Larrosa I., Henderson D.A., Oldham J., Burton A.J., and Barrett A.G.M. Org. Lett. 7 (2005) 4549-4552
16. Shaikh T.M.A., Emmanuvel L., and Sudalai A. J. Org. Chem. 71 (2006) 5043-5046
17. Khan A.T., and Goswami P. Tetrahedron Lett. 46 (2005) 4937-4940
18. Khan A.T., Goswami P., and Choudhury L.H. Tetrahedron Lett. 47 (2006) 2751-2754
19. 2 (150.18): C, 71.98; H, 6.71. Found: C, 71.72; H, 6.79.
20. Dakka J., and Sasson Y. J. Chem. Soc., Chem. Commun. (1987) 1421-1422
21. Barhate N.B., Gajare A.S., Wakharkar R.D., and Bedekar A.V. Tetrahedron 55 (1999) 11127-11142