Catalytic Friedel-Crafts allylation using Zn(II) triflimidate

Comptes Rendus Chimie

Volumn 12, Issue 8, 2009, Pages 916-921

  Ricci, Jérémy ^a   Poulain Martini, Sophie ^a   Duñach, Elisabet ^a  

^a UNIVERSITÉ CÔTE D'AZUR   (France)

Author keywords

Allylation; Catalysis; Friedel Crafts; Lewis acid; Metal trifluoromethanesulfonates; Prenyl acetate; Zinc bis(trifluoromethylsulfonyl)amide

Indexed keywords

EID: 67649687523     PISSN: 16310748     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.crci.2008.09.023     Document Type: Article

References (29)

1. Boelens H. Indian Perfumer 12 (1968) 28
2. Asakawa Y. Natural Product Commun. 3 (2008) 77
3. Chaieb K., Hajlaoui H., Zmantar T., Ben Kahla-Nakbi A., Rouabhia M., Mahdouani K., and Bakhrouf A. Phytother. Res. 21 (2007) 501
4. Tachibana Y. Chem. Lett. 8 (1977) 901
5. Min J.-H., Lee J.-S., Yang J.-D., and Koo S. J. Org. Chem. 68 (2003) 7925
6. Koncos R., and Friedmann B.S. In: Olah G.H. (Ed). Friedel-Crafts and Related Reactions vol. II (1963), Interscience, New York 289 part 1
7. Smith K., and Pollaud G. J. Chem. Soc., Perkin Trans. 1 24 (1994) 3519
8. Karade N., Shirodkar S., and Potrekar R. J. Chem. Res. (S) 10 (2003) 652
9. Kodomari M., Nawa S., and Miyoshi T. J. Chem. Soc., Chem. Commun. 18 (1995) 1895
10. Ichihara J. Chem. Commun. 19 (1997) 1921
11. Nishibayashi Y., Yamanashi M., Takagi Y., and Hidai M. Chem. Commun. 9 (1997) 859
12. Malkov A., Davis S., Baxendale I., Mitchell W., and Kocovsky P. J. Org. Chem. 64 (1999) 2751
13. Tada Y., Satake A., Shimizu I., and Yamamoto A. Chem. Lett. 12 (1996) 1021
14. Shimizu I., Sakamoto T., Kawaragi S., Maruyama Y., and Yamamoto A. Chem. Lett. 2 (1997) 137
15. Tsukada N., Yagura Y., Sato T., and Inoue Y. Synlett 10 (2003) 1431
16. Le Bras J., and Muzart J. Tetrahedron 63 (2007) 7942
17. Araki S., Manabe S.I., and Butsugan Y. Chem. Lett. 6 (1982) 797
18. Tsuchimoto T., Tobita K., Hiyama T., and Fukuzawa S.I. Synlett 6 (1996) 557
19. Tsuchimoto T., Tobita K., Hiyama T., and Fukuzawa S.I. J. Org. Chem. 62 (1997) 6997
20. Shiina I., and Suzuki M. Tetrahedron Lett. 43 (2002) 6391
21. Favier I., and Duñach E. Tetrahedron Lett. 44 (2003) 2031
22. E. Duñach-Clinet, I. Favier, D. Hebrault, J.R. Desmurs, Rhodia Chimie, FR Patent, FR 2818994 A1 20020705, 20001229.
23. Rojas-Oviedo I., Cardenas J., Marquez C., and Twyman L. J. Mex. Chem. Soc. 49 (2005) 10
24. Wang Y., Wu J., and Xia P. Synth. Commun. 36 (2006) 2685
25. Ortar G. Tetrahedron Lett. 44 (2003) 4311
26. Karade N., Shirodkar S., and Potrekar R. J. Chem. Res. Synop. 10 (2003) 652
27. Heinrich M., Blank O., Ullrich D., and Kirschstein M. J. Org. Chem. 72 (2007) 9609
28. Butsugan Y., Nagai K., Nagaya F., Tabuchi H., Yamada K., and Araki S. Bull. Chem. Soc. Jpn. 61 (1988) 1707
29. Bouzbouz S., and Kirschleger B. Synthesis 7 (1994) 714