Chromium-catalyzed oxidation of benzylcyclopropane with tert-butyl hydroperoxide

Catalysis Communications

Volumn 7, Issue 8, 2006, Pages 563-565

  Ajjou, Abdelaziz Nait ^a   Riahi, Abdelkhalek ^a   Chatterjee, Debabrata ^a,b   Muzart, Jacques ^a  

^a UNIVERSITÉ DE REIMS CHAMPAGNE ARDENNE   (France)

^b CSIR CENTRAL MECHANICAL ENGINEERING RESEARCH INSTITUTE   (India)

Author keywords

Benzylcyclopropane; Benzylic oxidation; Catalysis; Chromium oxide; tert Butyl hydroperoxide

Indexed keywords

CATALYSIS; CATALYST SELECTIVITY; CHROMIUM; KETONES; OXIDATION; PEROXIDES; REACTION KINETICS; SOLUTIONS;

BENZYLCYCLOPROPANE; BENZYLIC OXIDATION; CHROMIUM OXIDE; TERT-BUTYL HYDROPEROXIDE;

AROMATIC HYDROCARBONS;

EID: 33745731595     PISSN: 15667367     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.catcom.2006.01.021     Document Type: Article

References (28)

1. For reviews, see. Muzart J. Chem. Rev. 92 (1992) 113-140
2. Muzart J. Synthesis (1993) 11-27
3. Muzart J. Synthesis (1995) 1325-1347
4. Muzart J. Tetrahedron Lett. 28 (1987) 2131-2132
5. Muzart J., and N'Ai{dotless}̈t Ajjou A.J. Mol. Catal. 66 (1991) 155-161
6. Muzart J., and N'Ai{dotless}̈t Ajjou A. In: Barton D.H.R., Martell A.R., and Sawyer D.T. (Eds). The Activation of Dioxygen and Homogeneous Catalytic Oxidation (1993), Plenum Press, New York 471
7. Muzart J., and N'Ai{dotless}̈t Ajjou A. J. Mol. Catal. 92 (1994) 277-283
8. Boitsov S., Riahi A., and Muzart J. C.R. Acad. Sci. Paris, Série IIc 3 (2000) 747-750
9. Boitsov S., Songstad J., and Muzart J. J. Chem. Soc., Perkin Trans. II (2001) 2318-2323
10. Muzart J., and N'Ai{dotless}̈t Ajjou A. J. Mol. Catal. 92 (1994) 141-147
11. Barton D.H.R., Halley F., Ozbalik N., and Mehl W. Tetrahedron Lett. 30 (1989) 6615-6618
12. Inchley P., Lindsay Smith J.R., and Lower R.J. New. J. Chem. 13 (1989) 669-676
13. Masnovi J., Samsel E.G., and Bullock R.M. J. Chem. Soc., Chem. Commun. (1989) 1044-1045
14. Bowry V.W., Lusztyk J., and Ingold K.U. J. Chem. Soc., Chem. Commun. (1990) 923-925
15. Bowry V.W., and Ingold K.U. J. Am. Chem. Soc. 113 (1991) 5699-5707
16. Halgren T.A., Roberts J.D., Horner J.H., Martinez F.N., Tronche C., and Newcomb M. J. Am. Chem. Soc. 122 (2000) 2988-2994
17. Hollis R., Hughes L., Bowry V.W., and Ingold K.U. J. Org. Chem. 57 (1992) 4284-4287
18. Bullock R.M., and Samsel E.G. J. Am. Chem. Soc. 112 (1990) 6886-6898
19. Beckwith A.L.J., and Bowry V.W. J. Am. Chem. Soc. 116 (1994) 2710-2716
20. Tsuchii K., Imura M., Kamada N., Hirao T., and Ogawa A. J. Org. Chem. 69 (2004) 6658-6665
21. Muzart J. Tetrahedron Lett. 28 (1987) 2133-2134
22. Muzart J., and N'Ai{dotless}̈t Ajjou A. Synthesis (1993) 785-787
23. N'Ai{dotless}̈t Ajjou A., Muzart J., Savelon L., and Guillaumet G. Synthesis (1994) 359-360
24. 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
25. 0 species can effectively promote the oxidation of 1 with oxygen:. Mori K., Hara T., Mizugaki T., Ebitani K., and Kaneda K. J. Am. Chem. Soc. 126 (2004) 10657-10666
26. Collins C.J., Hanack M., Stutz H., Auchter G., and Schoberth W. J. Org. Chem. 48 (1983) 5260-5268
27. Pierre J.-L., Perraud R., and Arnaud P. Bull. Soc. Chim. Fr. (1969) 1322-1325
28. Leeper F.J., and Padmanabhan P. Tetrahedron Lett. 30 (1989) 5017-5020