N-methylpyrrolidine-2-one hydrotribromide: An efficient and new catalyst for the aziridination of alkenes using Chloramine-T under solvent free conditions

Journal of Molecular Catalysis A: Chemical

Volumn 256, Issue 1-2, 2006, Pages 16-20

  Jain, Suman L ^a   Joseph, Jomy K ^a   Sain, Bir ^a  

^a CSIR INDIAN INSTITUTE OF PETROLEUM   (India)

Author keywords

Aziridination; Chloramine T; MPHT; Olefins

Indexed keywords

AMINATION; AMINES; BROMINE COMPOUNDS; CATALYSIS; REACTION KINETICS; SOLVENTS;

AZIRIDINATION; CHLORAMINE-T; N-METHYLPYRROLIDIN-2-ONE HYDROTRIBROMIDE (MPHT); SOLVENT FREE CONDITION;

CATALYST ACTIVITY;

EID: 33747356553     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2006.04.029     Document Type: Article

References (30)

1. Muller P., and Fruit C. Chem. Rev. 103 (2003) 2905
2. Padwa A., and Woolhouse A.D. Aziridines and fused ring derivatives. In: Lwowski W. (Ed). Comprehensive Heterocyclic Chemistry vol. 7 (1984), Pergamon, Oxford 47-93
3. Kasai M., and Kono M. Synlett (1992) 778
4. Padwa A., and Woolhouse A.D. In: Katritzky A.R., and Rees C.W. (Eds). Comprehensive Heterocyclic Chemistry: The Structure Reactions and Synthesis and Uses of Heterocyclic Compounds vol. 7 (1984), Pergamon Press, Oxford 47
5. Kemp J.E. In: Trost B.M., and Fleming I. (Eds). Comprehensive Organic Synthesis vol. 7 (1991), Pergamon, Oxford 469
6. Yamada Y., Yamamoto T., and Okawara M. Chem. Lett. (1975) 361
7. Evans D.A., Faul M.M., Bilodeau M.T., Anderson B.A., and Barnes D.M. J. Am. Chem. Soc. 115 (1993) 5328
8. Ilewellyn D.B., Adamson D.M., and Amdtsen B.A. Org. Lett. 2 (2000) 4165
9. Ando T., Minakata S., Ryu I., and Komatsu M. Tetrahedron Lett. 39 (1998) 309
10. Ando T., Kano D., Minakata S., Ryu I., and Komatsu M. Tetrahedron 54 (1998) 13485
11. Kano D., Minakata S., and Komatsu M. J. Chem. Soc. Perkin Trans. (2001) 3186
12. Thakur V.V., and Sudalai A. Tetrahedron Lett. 44 (2003) 989
13. Jain S.L., Sharma V.B., and Sain B. Tetrahedron Lett. 45 (2004) 8731
14. Wu H., Xu C.-G., Ge J., and Yang L. Synth. Commun. 35 (2005) 1413
15. Simkhovich L., and Gross Z. Tetrahedron Lett. 42 (2001) 8089
16. Mondal E., Sahu P.R., Bose G., and Khan A.T. Tetrahedron Lett. 43 (2002) 2843
17. Chaudhuri M.K., Khan A.T., Patel B.K., Dey D., Kharmawophlang W., Lakshmiprabha T.R., and Mandal G.C. Tetrahedron Lett. 39 (1998) 8163
18. Fieser L.F., and Fieser M. Reagents for Organic Synthesis (1967), John Wiley, New York pp. 967
19. Cattaway F.D., and Hoyle G. J. Chem. Soc. (1923) 654
20. Avramoff M., Weiss J., and Schaechter O. J. Org. Chem. 28 (1963) 3256
21. Kajianeshi S., Tokiyama H., and Okamoto T. Chem. Lett. (1987) 627
22. Kar G., Saikia A.K., Bora U., Dehury S.K., and Chaudhuri M.K. Tetrahedron Lett. 44 (2003) 4503
23. Jeong J.U., Tao B., Sagasser I., Henniges H., and Sharpless K.B. J. Am. Chem. Soc. 120 (1998) 6844
24. Ali S.I., Nikalje M.D., and Sudalai A. Org. Lett. (1999) 705
25. Rogers R.D., and Seddon K.R. Science 302 (2003) 792
26. Seddon K.R. Nature 2 (2003) 363
27. Welton T. Chem. Rev. 99 (1999) 2071
28. Dupont J., de Suza R.F., and Suarez P.A.Z. Chem. Rev. 102 (2002) 3667
29. Bekaert A., Provot O., Rasolojaona O., Alami M., and Brion J.D. Tetrahedron Lett. 46 (2005) 4187
30. Evans D.A., Bilodeau M.T., and Faul M.M. J. Am. Chem. Soc. 116 (1994) 2742