Chemoselectivity of cobalt-catalysed carbonylation-A reliable platform for the synthesis of fluorinated benzoic acids

Journal of Fluorine Chemistry

Volumn 131, Issue 1, 2010, Pages 81-85

  Boyarskiy, Vadim P ^a   Fonari, Marina S ^b   Khaybulova, Tatiana S ^a   Gdaniec, Maria ^c   Simonov, Yurii A ^b  

^a ST PETERSBURG STATE UNIVERSITY   (Russian Federation)

^b INSTITUTE OF APPLIED PHYSICS   (Moldova)

^c ADAM MICKIEWICZ UNIVERSITY   (Poland)

Author keywords

Aryl halides; Carbonylation; Cobalt carbonyl; Crystal structure; Fluorinated benzoic acids

Indexed keywords

EID: 71249099036     PISSN: 00221139     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jfluchem.2009.10.010     Document Type: Article

References (33)

1. Heck R.F., and Breslow D.S. J. Am. Chem. Soc. 85 (1963) 2779-2782
2. Zucchi C., Palyi G., Sampar-Szerencses E., Galamb V., Marko L., Alper H., Januszkiewicz K., and Li F. Organometallics 15 (1996) 3222-3231
3. Zucchi C., Cornia A., Kleipeter E., Alper H., and Palyi G. J. Organomet. Chem. 586 (1999) 106-109
4. Alper H., Bencze L., and Boese R. J. Mol. Catal. A: Chem. 204/205 (2003) 227-233
5. Brunet J.J., Sidot C., Caubere P., and Loubinoux B. J. Org. Chem. 44 (1979) 2199-2202
6. Marchal J., Bodiguel J., Fort Y., and Caubere P. J. Org. Chem. 60 (1995) 8336-8340
7. Francalanci F., Foa M., Gardano A., and Bencini E. J. Organomet. Chem. 285 (1985) 293-303
8. Francalanci F., and Foa M. J. Mol. Catal. 41 (1987) 89-107
9. Miura M., Itoh K., and Nomura M. J. Mol. Catal. 48 (1988) 11-13
10. Zhesko T.E., Boyarskii V.P., and Beletskaya I.P. Metalloorg. Khim. (Russ.) 2 (1989) 385-387
11. Boyarskii V.P., Zhesko T.E., and Lanina S.A. Russ. J. Appl. Chem. 78 (2005) 1844-1848
12. Boyarskii V.P., Zhesko T.E., Larionov E.B., and Polukeev V.A. Russ. J. Appl. Chem. 80 (2007) 571-575
13. Boyarskii V.P., Larionov E.B., Polyakova S.M., Boyarskaya I.A., and Zhesko T.E. Russ. J. Gen. Chem. 77 (2007) 915-922
14. Boyarskii V.P. Russ. J. Gen. Chem. 78 (2008) 1742-1753
15. Galamb V., and Palyi G. Atti. Acad. Sci. Bologna Rend. Cl. Sci. Fis. 270 (1982) 157-172
16. Palyi G., Galamb V., Ungvary F., and Marko L. Coord. Chem. Rev. 53 (1984) 37-53
17. Rodriguez J.R., Agejas J., and Bueno A.B. Tetrahedron Lett. 47 (2006) 5661-5663
18. Rossi R.A., Pierini A.B., and Penenory A.B. Chem. Rev. 103 (2003) 71-167
19. Shi M., and Feng Y.-S. J. Org. Chem. 66 (2001) 3235-3237
20. Berger P., Bessmernykh A., Caille J.-C., and Mignonac S. Synthesis 18 (2006) 3106-3110
21. Gohier F., Castanet A.-S., and Mortier J. J. Org. Chem. 70 (2005) 1501-1504
22. Soloski E.J., and Tamborski C. J. Organomet. Chem. 157 (1978) 373-377
23. Kraay G.M. Rec. Trav. Chim. Pays-Bas 49 (1930) 1082-1092
24. Gdaniec M., Jankowski W., Milewska M.J., and Połonski T. Angew. Chem. Int. Ed. 42 (2003) 3903-3906
25. Etter M. Acc. Chem. Res. 23 (1990) 120-126
26. Desiraju G.R., and Parthasarathy R. J. Am. Chem. Soc. 111 (1989) 8725-8726
27. Corradi E., Meille S.V., Messina M.T., Metrangolo P., and Resnati G. Angew. Chem. Int. Ed. 39 (2000) 1782-1786
28. Voth A.R., Khuu P., Oishi K., and Ho P.S. Nat. Chem. 1 (2009) 74-79
29. Sturm K., Siedel W., Weyer R., and Ruschig H. Chem. Ber. 99 (1966) 328-344
30. Ivanova V.M., Seina Z.N., Nemleva S.A., and Gitis S.S. Zh. Obshch. Khim. (Russ.) 36 (1966) 127-128
31. Oxford Diffraction CrysAlis CCD, Version 1.170 (2004), Oxford Diffraction Ltd, Abingdon, Oxfordshire, England
32. Oxford Diffraction CrysAlis RED, Version 1.171 (2005), Oxford Diffraction Ltd, Abingdon, Oxfordshire, England
33. Sheldrick G.M. SHELXS97 and SHELXL97, Programs for Crystal Structure Solution and Refinement (1997), University of Göttingen, Germany