Selectfluor™ F-TEDA-BF4 as a versatile mediator or catalyst in organic chemistry

Acta Chimica Slovenica

Volumn 52, Issue 1, 2005, Pages 13-26

  Stavber, Stojan ^a   Zupan, Marko ^a,b  

^a JO EF STEFAN INSTITUTE   (Slovenia)

^b UNIVERSITY OF LJUBLJANA   (Slovenia)

Author keywords

Allylstannation; Bromination; Deprotection; Hexametylbenzene; Iodination; Selectfluor F TEDA BF4

Indexed keywords

1,3 DITHIANE DERIVATIVE; ALDEHYDE DERIVATIVE; BENZENE DERIVATIVE; BENZYL DERIVATIVE; BENZYLIDENE DERIVATIVE; BORIC ACID; EPOXIDE; ETHER DERIVATIVE; IMINE; IODINE DERIVATIVE; ORGANIC COMPOUND; REAGENT; TETRAHYDROPYRAN DERIVATIVE;

BROMINATION; CATALYSIS; CATALYST; CHLORINATION; CYANATION; CYCLOADDITION; ELECTRIC ACTIVITY; FLUORINATION; IODINATION; MEDIATOR; NITRATION; ORGANIC CHEMISTRY; REVIEW; RING OPENING; SYNTHESIS;

EID: 17444368089     PISSN: 13180207     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (43)

1. Organofluorine Chemistry: Principles and Commercial Applications; R. E Banks, B. E. Smart, J. C. Tatlow, Eds.; Plenum Press: New York, 1994.
2. Chemistry of Organic Fluorine Compounds II: A Critical Review; M. Hudlicky, A. E. Pavlath, Eds.; ACS Monograph 187, American Chemical Society: Washington, DC, 1995.
3. Biomedicinal Frontiers of Fluorine Chemistry; I. Ojima, J. R. McCarthy, J. T. Welch, Eds.; ACS Symposium Series 693; American Chemical Society: Washington, DC, 1996.
4. Methods of Organic Chemistry (Houben-Weyl), 4th edition, Vols. E 10a-c: Organo-Fluorine Compounds; B. Baasner, H. Hagemann, J. C. Tatlow, Eds.; Thieme: Stuttgart, 1999.
5. Modern Fluoroorganic Chemistry. Synthesis, Reactivity, Applications; P. Kirsch, Ed.; Wiley: Weinheim, 2004.
6. M. Shimizu, T. Hiyama, Angew. Chem., Int. Ed. 2004, 44, 214-231.
7. M. Zupan. In Chemistry of Functional groups, Supplement D2: The Chemistry of Halides, pseudo-halides and azides, S. Patai, Z. Rappoport, Eds.; Wiley&Sons: New York, 1995; Chapter 15, 821-860.
8. S. Rozen, Chem Rev. 1996, 96, 1717-1736.
9. G. S. Lal, P. G. Pez, G. R. Syvret, Chem. Rev. 1996, 96, 1737-1755.
10. D. S. Taylor, C. C. Kotoris, G. Hum, Tetrahedron 1999, 55, 12431-12477.
11. G. G. Furin, A. A. Fainzilberg, Russ. Chem. Rev. 1999, 68, 653-684.
12. G. G. Furin, In Methods of Organic Chemistry (Houben-Weyl), 4th edition, Vol. E 10a: Organo-Fluorine Compounds; B. Baasner, H. Hagemann, C. J. Tatlow, Eds.; Thieme: Stuttgart, 1999, 432-498.
13. R. E. Banks, U.S. Patent 5 086 178, 1992.
14. R. E. Banks, N. S. Mohialdin-Khaffaf, G. S. Lal, I. Sharif, G. R. Syvret, Chem. Commun. 1992, 595-596.
15. M. Zupan, S. Stavber, in Trends in Organic Chemistry; Research Trends: Trivandrum, India, 1995, 5, 11-36.
16. R. E. Banks, J. Fluorine Chem. 1998, 87, 1-17.
17. R. P. Singh, J. M. Shreeve, Acc. Chem. Res. 2004, 37, 31-44.
18. P. T. Nyffeler, S. G. Duron, M. D. Burkart, S. P. Vincent, C-H. Wong, Angew. Chem., Int. Ed. 2004, 44, 192-212.
19. J. J. Hart, G. R. Syvret, J. Fluorine Chem. 1999, 100, 157-161.
20. M. Zupan, M. Papež, S. Stavber, J. Fluorine Chem. 1996, 78, 137-140.
21. G. Stavber, M. Zupan, M. Jereb, S. Stavber, Org. Lett. 2004, 6, 4973-4976.
22. G. P. Girina, A. A. Fainzil'berg, L. G. Feoktistov, Russ. J. Electrochem. 2000, 36, 162-163.
23. A. G. Gilicinski, G. P. Pez, R. G. Syvret, G. S. Lal, J. Fluorine Chem. 1992, 59, 157-162.
24. R. E. Banks, N. J. Lawrence, A. L. Popplewell, Synlett 1994, 831-832.
25. M. Zupan, J. Iskra, S. Stavber, Bull. Chem. Soc. Jpn. 1995, 68, 1655-1660.
26. S. Stavber, M. Jereb, M. Zupan, J. Phys. Org. Chem. 2002, 15, 56-61.
27. S. Stavber, M. Jereb, M. Zupan, Arkivoc 2001, (V), 98-107; http://www.arkat-usa.org/ark/journal/2001/I05_Tisler/160/MT-160B.pdf
28. M. Zupan, J. Iskra, S. Stavber, Tetrahedron Lett. 1997, 38, 6305-6306.
29. S. Stavber, P. Kralj, M. Zupan, Synlett 2002, 598-600.
30. S. Stavber, P. Kralj, M. Zupan, Synthesis 2002, 1513-1518.
31. C. Chiappe, D. Pieraccini, Arkivoc 2002, (XI), 249-255. http://www.arkat-usa.org/ark/journal/2002/I11_Spinelli/MS-574J/574J.pdf
32. S. Stavber, M. Jereb, M. Zupan, Chem. Commun. 2002, 488-489.
33. S. Stavber, M. Jereb, M. Zupan, Synthesis 2003, 853-858.
34. S. Stavber, M. Jereb, M. Zupan, Tetrahedron 2003, 59, 5935-5940.
35. C. Ye, J. M. Shreeve, J. Org. Chem. 2004, 69, 8561-8563.
36. R. G. Syvret, K. M. Butt, T. P. Nguyen, V. L. Bulleck, R. D. Rieth, J. Org. Chem. 2002, 67, 4487-4493.
37. S. Stavber, P. Kralj, M. Zupan, Synlett 2001, 1152-1154.
38. S. Stavber, P. Kralj, M. Zupan, Acta. Chim. Slov. 2002, 49, 553-560.
39. J. Liu, C-H. Wong, Tetrahedron Lett. 2002, 43, 3915-3919.
40. J. Liu, C-H. Wong, Tetrahedron Lett. 2002, 43, 4037-4039.
41. G. R. Krow, G. Lin, K. P. Moore, A. M. Thomas, C. DeBrosse, C. W. Ross, H. G. Ramjit, Org. Lett. 2004, 6, 1669-1672.
42. J. S. Yadav, B. V. S. Reddy, C. S. Reddy, Tetrahedron Lett. 2004, 45, 1291-1293.
43. J. S. Yadav, B. V. S. Reddy, V. Sunitha, C. S. Reddy, Adv. Synth. Catal. 2003, 345, 1203-1206.