Synthesis of new pentafluorosulfanylacrylates (F5SCH{double bond, long}CHCHO, F5SCH{double bond, long}CHCN, F5SCH{double bond, long}CHCOOCH3) and use of them as dienophiles in Diels-Alder reaction

Journal of Fluorine Chemistry

Volumn 128, Issue 7, 2007, Pages 862-867

  Brel, Valery K ^a  

^a INSTITUTE OF PHYSIOLOGICALLY ACTIVE COMPOUNDS   (Russian Federation)

Author keywords

Alkenes; Diels Alder; Fluorine; Sulfur

Indexed keywords

EID: 34250736211     PISSN: 00221139     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jfluchem.2007.04.013     Document Type: Article

References (17)

1. J.C. Hansen, P.M. Savu, United States Patent 5,159,105 (1992).
2. J.C. Hansen, P.M. Savu, United States Patent 5,286,352 (1992).
3. Winter R., Nixon P.G., Gard G.L., Castner D.G., Holcomb N.R., Hu Y.-H., and Grainger D.W. Chem. Mater. 11 (1999) 3044
4. Winter R., Nixon P.G., Terjeson R.J., Mohtasham J., Holcomb N.R., Grainger D.W., Graham D., Caster D.G., and Gard G.L. J. Fluorine Chem. 115 (2002) 107
5. Winter R., Dodean R., Holmes L., and Gard G.L. J. Fluorine Chem. 125 (2004) 37
6. Brel V.K. Synthesis (2006) 339
7. Winter R., and Gard G.L. J. Fluorine Chem. 66 (1994) 109
8. Trushkov I.V., and Brel V.K. Tetrahedron Lett. 46 (2005) 4777
9. Brel V.K. Synthesis (2005) 1245
10. Itoh K., Takahashi S., Ueki T., Sogiyama T., Takahashi T.T., and Horiuchi C.A. Tetrahedron Lett. 43 (2002) 7035
11. Grakautas V. J. Org. Chem. 38 (1973) 2999
12. Nixon P.G., Renn J., Terjeson R.J., Choi Y.S., Winter R., and Gard R. J. Fluorine Chem. 115 (1998) 13
13. In: Fringuelly F., and Taticchi A. (Eds). The Diels-Alder Reaction: Selected Practical Methods (2002), John Wiley & Sons, Ltd 122-123
14. Hoover F.W., and Coffman D.D. J. Org. Chem. 29 (1964) 3567
15. Dolbier R.W., Mitani A., Xu W., and Ghiviriga I. Org. Lett. 8 (2006) 5573
16. Brel V.K. Synthesis (2006) 2665
17. In: Fringuelly F., and Taticchi A. (Eds). The Diels-Alder Reaction: Selected Practical Methods (2002), John Wiley & Sons, Ltd 40-42