A novel method for the reduction of sulfoxides and pyridine N-oxides with the system silane/MoO2Cl2

Tetrahedron

Volumn 62, Issue 41, 2006, Pages 9650-9654

  Fernandes, Ana C ^a   Romão, Carlos C ^a  

^a INSTITUTO DE TECNOLOGIA QUÍMICA E BIOLÓGICA   (Portugal)

Author keywords

Dioxomolybdenum dichloride; Pyridine N oxides; Reduction; Sulfoxides

Indexed keywords

MOLYBDENUM COMPLEX; PYRIDINE 1 OXIDE; SILANE; SULFOXIDE;

ARTICLE; CATALYSIS; DEOXYGENATION; PRIORITY JOURNAL; REACTION ANALYSIS; REDUCTION; TEMPERATURE SENSITIVITY;

EID: 33748065967     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.07.077     Document Type: Article

References (23)

1. Madesclaire M. Tetrahedron 44 (1988) 6537 and references cited therein
2. Kukushkin V.Y. Coord. Chem. Rev. 139 (1995) 375 and references cited therein
3. Espenson J.H. Coord. Chem. Rev. 249 (2005) 329 and references cited therein
4. Raju B.R., Devi G., Nongpluh Y.S., and Saikia A.K. Synlett (2005) 358
5. Sanz R., Escribano J., Fernández Y., Aguado R., Pedrosa M.R., and Arnáiz F.J. Synthesis (2004) 1629
6. Harrison D.J., Tam N.C., Vogels C.M., Langler R.F., Baker R.T., Decken A., and Westcott S.A. Tetrahedron Lett. 45 (2004) 8493
7. Yoo B.W., Choi K.H., Kim D.Y., Choi K.I., and Kim J.H. Synth. Commun. 33 (2003) 53
8. Nicolaou K.C., Koumbis A.E., Snyder S.A., and Simonsen K.B. Angew. Chem., Int. Ed. 39 (2000) 2529
9. Yoo B.W., Choi J.W., and Yoon C.M. Tetrahedron Lett. 47 (2006) 125
10. Sanz R., Escribano J., Fernández Y., Aguado R., Pedrosa M.R., and Arnáiz F.J. Synlett (2005) 1389
11. Kumar S., Saini A., and Sandhu J.S. Tetrahedron Lett. 50 (2005) 8737
12. Ilias M., Barman D.C., Prajapati D., and Sandhu J.S. Tetrahedron Lett. 10 (2002) 1877
13. Wang Y., and Espenson J.H. Org. Lett. 2 (2000) 3525
14. Ram S.R., Chary K.P., and Iyengar D.S. Synth. Commun. 30 (2000) 3511
15. Chary K.P., Mohan G.H., and Iyengar D.S. Chem. Lett. (1999) 1339
16. Enemark J.H., Cooney J.J.A., Wang J.-J., and Holm R.H. Chem. Rev. 104 (2004) 1175 and references cited therein
17. Kisker C., Schindelin H., and Rees D. Annu. Rev. Biochem. 66 (1997) 233
18. Most K., Hoβbach J., Vidović D., Magull J., and Mösch-Zanetti N.C. Adv. Synth. Catal. 347 (2005) 463
19. Arnáiz F.J., Agudo R., Pedrosa M.R., and De Cian A. Inorg. Chim. Acta 347 (2003) 33
20. Arnáiz F.J., Agudo R., and Ilarduya J.M.M. Polyhedron 13 (1994) 3257
21. Fernandes A.C., Fernandes R., Romão C.C., and Royo B. Chem. Commun. (2005) 213
22. Fernandes A.C., and Romão C.C. Tetrahedron Lett. 46 (2005) 8881
23. Fernandes A.C., and Romão C.C. J. Mol. Catal A: Chem. 253 (2006) 96