Influence of substituents in the salicylaldehyde-derived Schiff bases on vanadium-catalyzed asymmetric oxidation of sulfides

Applied Organometallic Chemistry

Volumn 22, Issue 5, 2008, Pages 253-257

  Liu, Haibin ^b   Wang, Mei ^a,b   Wang, Ying ^b   Yin, Ran ^b   Tian, Wei ^b,c   Sun, Licheng ^b,d  

^a Dalian University of Technology ^*  (China)

^b DALIAN UNIVERSITY OF TECHNOLOGY   (China)

^c ASTRAZENECA R AND D   (Sweden)

^d ROYAL INSTITUTE OF TECHNOLOGY   (Sweden)

Author keywords

3 arylsalicylaldehyde; Asymmetric sulfoxidation; Chiral Schiff bases; Chiral sulfoxides; Vanadium catalyst

Indexed keywords

3-ARYLSALICYLALDEHYDE; ASYMMETRIC SULFOXIDATION; CHIRAL SCHIFF BASES; CHIRAL SULFOXIDES; VANADIUM CATALYST;

TRANSITION METALS;

EID: 51349108362     PISSN: 02682605     EISSN: 10990739     Source Type: Journal    
DOI: 10.1002/aoc.1386     Document Type: Article

References (33)

1. I. Fernande, N. Khiar, Chem. Rev. 2003; 103, 3651.
2. M. Kose, J. Photochem. Photobiol. A: Chem. 2004; 165, 97.
3. Z. Han, J. J. Song, N. K. Yee, Y. Xu, W. Tang, C. H. Senanayake, Org. Process Res. Devl. 2007; 11, 605.
4. R. Bentley, Chem. Soc. Rev. 2005; 34, 609.
5. A. Korte, J. Legros, C. Bolm, Synlett 2004; 13, 2397.
6. P. Pitchen, H. B. Kagan, Tetrahedron Lett. 1984; 25, 1049.
7. H. Cotton, T. Elebring, M.Larsson, L. Li, H. Sörensen, Tetrahedron: Asymmetry 2000; 11, 3819.
8. S. Schoumacker, O. Hamelin, S. Téti, J. Pécaut, M. Fontecave, J. Org. Chem. 2005; 70, 301.
9. A. D. Franklin, R. T. Reddy, P. J. Carroll, J. Am. Chem. Soc. 1992; 114(4), 1428.
10. J. T. Groves, P. Viski, J. Org, Chem. 1990; 55, 3628.
11. Y. Naruta, F. Tani, K. Marayama, J. Chem. Soc., Chem. Commun. 1990; 1378.
12. T. Katsuki, Coord. Chem. Rev. 1995; 140, 189.
13. M. Cavazzini, G. Pozzi, S. Quici, I. Shepperson, J. Mol. Catal. A: Chem. 2003; 204-205, 433.
14. X. Wang, X. Wang, K. L. Ding, Chem. Eur. J. 2005; 11, 4078.
15. L. J. P. Martyn, S. Pandarajy, A. K. Yudin, J. Organomet. Chem. 2000; 98, 603.
16. M. I. Donnoli, S. Superchi, C. Rosini, J. Org. Chem. 1998; 63, 9392.
17. M. I. Superchi, C. Rosini, Tetrahedron: Asymmetry 1997; 8, 349.
18. M. Bonchio, G. Licini, F. Di Furia, S. Manotovani, G. Modena, W. Nugent, J. Org. Chem. 1999; 64, 1326.
19. B. Pelotier, M. S. Anson, I. B. Campbell, Synlett 2002; 7, 1055.
20. Y. C. Jeong, S. Choi, Y. D. Hwang, K. H. Ahn, Tetrahedron Lett. 2004; 45, 9249.
21. [21 ] Ah. Vetter, A. Berkessel, Tetrahedron Lett. 1998; 39, 1741.
22. J. Legros, C. Bolm, Angew. Chem. Int. Edn 2004; 43, 4225.
23. C. Bolm, F. Bienewald, Angew. Chem. Int. Edn Engl. 1995; 34, 2640.
24. A. Barbarini, R. Maggi, M. Muratori, G. Sartori, R. Sartorio, Tetrahedron: Asymmetry 2004; 15, 2467.
25. C. Bolm, F. Bienewald, Synlett. 1998; 1327.
26. A. Gao, M. Wang, D. Wang, L. Zhang, H. Liu, W. Tian, L. Sun, Chin. J. Catal. 2006; 27(8), 743.
27. H. Liu, M. Wang, Y. Wang, L. Sun, Synth. Commun. 2007; 37, 3815.
28. G. F. Hennion, G. J. Anderson, J. Am.Chem. Soc. 1946; 68, 424.
29. J. Legros, C. Bolm, Chem. Eur. J. 2005; 11, 1086.
30. N. N. Karpyshev, O. D. Yakovleva, E. P. Talsi, J. Mol. Catal. A: Chem. 2000; 157, 91.
31. K. Kaczorowska, Z. Kolarska, K. Mitka, P. Kowalski, Tetrahedron 2005; 61, 8315.
32. M. J. Mckennon, A. I. Meyers, J. Org. Chem. 1993; 58, 3568.
33. Y. Zhang, M. Hao, H. Wang, X. Lv, Dyestuffs and Coloration 2004; 41, 284.