A rhodium-catalyzed heterocycloaddition route to 5-fluoroalkyl substituted 1,3-oxazoles

Journal of Fluorine Chemistry

Volumn 103, Issue 2, 2000, Pages 139-144

  Wang, Yanli ^a   Zhu, Shizheng ^a  

^a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

1,3 oxazoles; Ethyl 2 diazo fluoroalkylacetoacetate; Nitriles; Perfluoroalkanesulfonyl azide; Rhodium catalyzed

Indexed keywords

EID: 0041724973     PISSN: 00221139     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-1139(99)00306-1     Document Type: Article

References (23)

1. I.J. Turshi (Ed.), Oxazoles Wiley, New York, 1986.
2. Giambattista M.D., Chinali G., Cocito C. J. Antimicrob. Chemoth. 24:1989;485.
3. Wolbers P., Misske A.M., Hoffmann H.R. Tetrahedron Lett. 40:1999;4527.
4. Evans D.A., Gage J.R., Leighton J.L., Kim A.S. J. Org. Chem. 57:1992;1961.
5. Williams E.L. Tetrahedron Lett. 33:1992;1033.
6. Connell R.D., Tebbe M., Gangloff A.R., Helquiet P. Tetrahedron. 49:1993;5445.
7. Bagley M.C., Buck R.T., Hind S.L., Moody C.J. J. Chem. Soc. Perkin Trans I. 3:1998;591.
8. Wolbers P., Misske A.M., Hoffmann H.M.R. Tetrahedron Lett. 40:1999;4527.
9. Doyle K.J., Moody C.J. Tetrahedron Lett. 33:1992;7769.
10. G.Q. Shi, Y.Y. Xu, J. Chem. Soc. Chem Commun. (1989) 607.
11. Chambers R.D., Sarget C.R. Adv. Heterocycle Chem. 1:1981;28.
12. Shozo F., Hiroshi K., Takashj O. Nogoya Kogyo GiJutsu Shikensho Hokoku. 35(3):1986;108 (in Japanese).
13. Doering W.V.E., Depuy C.H. J. Am. Chem. Soc. 75:1953;5955.
14. M. Regitz, G. Maas (Eds.), Diazo Compounds: Properties and Synthesis, Academic Press, New York, 1986, p. 326.
15. Weygand F., Bestmann H.J. Angew. Chem. 72:1960;538.
16. Zhu S.Z., Xu G.L., Qin C.Y., Xu Y., Chu Q.L. Chinese J. Chem. 16:1998;264.
17. Zhu S.Z., Xu G.L., Qin C.Y., Xu Y., Chu Q.L. Phosphorus, Sulfur, Silicon. 5:1998;1.
18. Iznaden M., Portella C. J. Fluorine. Chem. 43:1989;105.
19. Doyle M.P. Chem. Rev. 86:1986;919.
20. Doyle M.P., Buhro W.E. J. Org. Chem. 45:1980;3657.
21. Hoffmann M.G., Wenkert E. Tetrahedron. 49:1993;1057.
22. Regitz M., Hocker J., Liedhegener A. Org. Synth. 48:1968;36.
23. S.Z. Zhu, J. Chem. Soc. Perkin Trans I. (1994) 2077.