In(OTf)3-catalyzed thiolysis of 1,2-epoxides by arylthiols under SFC. A new approach for the synthesis of thiazolopyridinium ionic liquids

Green Chemistry

Volumn 8, Issue 1, 2006, Pages 191-196

  Fringuelli, Francesco ^a   Pizzo, Ferdinando ^a   Tortoioli, Simone ^a   Zuccaccia, Cristiano ^a   Vaccaro, Luigi ^a  

^a UNIVERSITY OF PERUGIA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 33645452311     PISSN: 14639262     EISSN: 14639270     Source Type: Journal    
DOI: 10.1039/b514979g     Document Type: Article

References (43)

1. J. H. Clark Green Chem. 1999 1 1-8.
2. Green Chemistry: Challenging Perspectives, ed. P. Tundo and P. T. Anastas, Oxford Science, Oxford, 1999.
3. Various authours Pure Appl. Chem. 2001 73 77-199.
4. For recent papers see: F. Fringuelli F. Pizzo L. Vaccaro J. Org. Chem. 2001 66 4719-4722.
5. F. Fringuelli F. Pizzo S. Tortoioli L. Vaccaro Adv. Synth. Catal. 2002 344 379-384.
6. F. Fringuelli F. Pizzo M. Rucci L. Vaccaro J. Org. Chem. 2003 68 7041-7045.
7. F. Fringuelli F. Pizzo S. Tortoioli L. Vaccaro Green Chem. 2003 5 436-440.
8. D. Amantini F. Fringuelli O. Piermatti F. Pizzo L. Vaccaro J. Org. Chem. 2003 68 9263-9268.
9. D. Amantini F. Fringuelli F. Pizzo S. Tortoioli L. Vaccaro Synlett 2003 2292-2296.
10. F. Fringuelli F. Pizzo S. Tortoioli L. Vaccaro J. Org. Chem. 2003 68 8248-8251.
11. F. Fringuelli F. Pizzo L. Vaccaro J. Org. Chem. 2004 69 2315-2321.
12. D. Amantini F. Fringuelli F. Pizzo L. Vaccaro J. Org. Chem. 2001 66 6734-6737.
13. F. Fringuelli F. Pizzo S. Tortoioli L. Vaccaro Tetrahedron Lett. 2003 44 6785-6787.
14. D. Amantini R. Beleggia F. Fringuelli F. Pizzo L. Vaccaro J. Org. Chem. 2004 69 2896-2898.
15. F. Fringuelli F. Pizzo S. Tortoioli L. Vaccaro J. Org. Chem. 2004 69 7745-7747.
16. F. Fringuelli F. Pizzo C. Vittoriani L. Vaccaro Chem. Commun. 2004 2756-2757.
17. F. Fringuelli F. Pizzo S. Tortoioli L. Vaccaro J. Org. Chem. 2004 69 8780-8785.
18. D. Amantini F. Fringuelli F. Pizzo J. Org. Chem. 2002 67 7238-7243.
19. D. Amantini F. Fringuelli O. Piermatti F. Pizzo L. Vaccaro J. Org. Chem. 2003 68 9263-9268.
20. J. D. Holbrey K. R. Seddon Clean Prod. Process. 1999 1 223-236.
21. T. Welton Chem. Rev. 1999 99 2071-2083.
22. P. Wasserscheid W. Keim Angew. Chem., Int. Ed. 2000 39 3772-3789.
23. C. Baudequin J. Baudoux J. Levillain D. Cahard A. –C. Gaumont J. –C. Plaquevent Tetrahedron: Asymmetry 2003 14 3081-3093.
24. J. Levillain G. Dubat I. Abrunhosa M. Gulea A. –C. Gaumont Chem. Commun. 2003 2914-2915.
25. Enantiopure monosubstituted 1,2-epoxides are easily prepared in multi-ton quantities by Jacobsen hydrolytic kinetic resolution of racemates: M. Tokunaga J. F. Larrow F. Kakiuchi E. Jacobsen Science 1997 277 936-938.
26. 4].
27. A. E. Vougioukas H. B. Kagan Tetrahedron Lett. 1987 28 6065-6068 [Lanthanides complexes].
28. 2O].
29. 3].
30. 4].
31. 4].
32. 2].
33. 3].
34. 3].
35. N. Devan P. R. Sridhar K. R. Prabhu S. Chandrasekaran J. Org. Chem. 2002 67 9417-9420 [tetrathiomolybdate].
36. 3B].
37. D. A. Evans D. M. Barnes J. S. Johnson T. Lectka P. von Matt S. J. Miller J. A. Murry R. D. Norcross E. A. Shaughnessy K. R. Campos J. Am. Chem. Soc. 1999 121 7582-7594.
38. A. Fürstner M. Libl C. W. Lehmann M. Picquet R. Kunz C. Bruneau D. Touchard P. H. Dixneuf Chem. Eur. J. 2000 6 1847-1857.
39. 2 which gave complete conversion after 0.5 h.
40. 6 as counterions).
41. G. L. Rebeiro B. M. Khadilkar Synthesis 2001 370-372.
42. L. Magna Y. Chauvin G. P. Niccolai J. –M. Basset Organometallics 2003 22 4418-4425.
43. A. R. Katritzky O. Rubio M. Szajda B. Nowak-Bydra J. Chem. Res. (S) 1984 234-235.