Alumina supported copper nanoparticles for aziridination and cyclopropanation reactions

Catalysis Communications

Volumn 8, Issue 12, 2007, Pages 1963-1968

  Lakshmi Kantam, M ^a   Swarna Jaya, V ^a   Jaya Lakshmi, M ^a   Reddy, B Ramachandra ^a   Choudary, B M ^b   Bhargava, S K ^c  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

^b Ogene Systems I Pvt Ltd   (India)

^c RMIT UNIVERSITY   (Australia)

Author keywords

Alumina; Aziridination; Copper nanoparticles; Cyclopropanation; Reusability

Indexed keywords

ALUMINA; CATALYST ACTIVITY; CENTRIFUGATION; COPPER; OLEFINS;

AZIRIDINATION; COPPER NANOPARTICLES; CYCLOPROPANATION;

NANOPARTICLES;

EID: 35548941409     PISSN: 15667367     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.catcom.2007.03.012     Document Type: Article

References (33)

1. In: Ojima I. (Ed). Catalytic Asymmetric Synthesis. second ed. (2000), Wiley VCH, New York
2. Doyle M.P. Chem. Rev. 86 (1986) 919
3. Salaun J. Chem. Rev. 89 (1989) 1247
4. Evans D.A., Faul M.M., and Bilodeau M.T. J. Am. Chem. Soc. 116 (1994) 2742
5. Gillespie K.M., Crust E.J., Deeth R.J., and Scott P. J. Chem. Soc. Chem. Commun. (2001) 785
6. Gullick J., Taylor S., Kerton O., McMorn P., King F., Hancock F.E., Bethell D., Bulman Page P.C., and Hutchings G.J. Catal. Lett. 75 (2001) 151
7. Zhang J.L., and Che C.M. Org. Lett. 4 (2002) 1911
8. Vyas R., Chanda B.M., Belhekar A.A., Patel D.R., Rain R.N., and Bedekar A.V. J. Mol. Catal. A 160 (2000) 237
9. Mar Diaz-Requejo M., and Perez P.J. J. Organomet. Chem. 617-618 (2001) 110
10. Kantam M.L., Kavitha B., Neeraja V., Haritha Y., Chaudhuri M.K., and Dehury S.K. Synlett (2004) 525
11. Callot H.J., and Metz F. Tetrahedron 41 (1985) 4495
12. Seitz W.J., and Hossain M.M. Tetrahedron Lett. 35 (1994) 7561
13. Anciaux A.J., Hubert A.J., Noels A.F., Petiniot N., and Teyssie P. J. Org. Chem. 45 (1980) 695
14. Hildebrand J.P., and Marsden S.P. Synlett (1996) 893
15. Tamblyn W.H., Hoffmann S.R., and Doyle M.P. J. Organomet. Chem. 216 (1981) C64-C68
16. Nakamura A., Yoshida T., Cowie M., Otsuka S., and Ibers J.A. J. Am. Chem. Soc. 99 (1977) 2108
17. Boverie S., Simal F., Demonceau A., and Noels A.F. Tetrahedron Lett. 38 (1997) 7543
18. Finta Z., Hell Z., Balán D., Cwik A., Kemény S., and Figueras F. J. Mol. Catal. A: Chem. 161 (2000) 149
19. Fuson R.C., and Cleveland E.A. Organic Syntheses III (1995), Wiley, New York 339
20. Fraile J.M., Garcia B., Iarcia J., Mayoral J.A., and Figueras F. Heterogen. Catal. Fine Chem. IV (1997) p. 57
21. Sun W., Xia C.-G., and Wang H.-W. New J. Chem. 26 (2002) 755
22. Wang H., Sun W., and Xia C. J. Mol. Catal. A: Chem. 206 (2003) 199
23. Alcon M.J., Corma A., Iglesias M., and Sanchez F. J. Organomet. Chem. 655 (2002) 134
24. Liu X., Liu Y., Li X., Xiang S., Zhang Y., Ying P., Wei Z., and Li C. Appl. Catal. A: Gen. 239 (2003) 279
25. Sacco L., Lambert S., Pirard J.-P., and Noels A.F. J. Catal. 232 (2005) 51
26. Kantam M.L., Haritha Y., Reddy N.M., Choudary B.M., and Figueras F. Catal. Lett. 83 (2002) 187
27. Reetz M.T., and Westermann E. Angew. Chem. 39 (2000) 165
28. Son S.U., Park I.K., Park J., and Hyeon T. Chem. Commun. (2004) 778-779
29. Pachón L.D., van Maarseveen J.H., and Rothenberg G. Adv. Synth. Catal. 347 (2005) 811
30. Verma A.K., Kumar R., Chaudhary P., Saxena A., Shankar R., Mozumdar S., and Chandra R. Tetrahedron Lett. 46 (2005) 5229
31. Lakshmi Kantam M., Swarna Jaya V., Sreedhar B., Mohan Rao M., and Choudary B.M. J. Mol. Cat. A: Chem. 256 (2006) 273
32. White R.E., and McCarthy M.B. J. Am. Chem. Soc. 106 (1984) 4922
33. Velu S., and Swamy C.S. Appl. Catal. A: Gen. 145 (1996) 141