5-Perfluoroalkylpyrazoles 6, 5-perfluoroalkylisoxazoles 11, and 4-perfluoroacylisoxazoles 13 are obtained in high chemical yields and complete site and regioselectivity through the reaction of β-perfluoroalkyl-β-dicarbonyls 2 with hydrazonyl halides 1 and halooximes 8 in the presence of bases. β-Perfluoroalkyl-β-dicarbonyls 2 are shown to be convenient precursors of 5-perfluoroalkypyrazoles 6, 5-perfluoroalkylisoxazoles 11, and 4-perfluoroacylisoxazoles 13.

An efficient entry to perfluoroalkyl substituted azoles starting from β-perfluoroalkyl-β-dicarbonyl compounds

BRAVO, PIERFRANCESCO;RESNATI, GIUSEPPE
1994-01-01

Abstract

5-Perfluoroalkylpyrazoles 6, 5-perfluoroalkylisoxazoles 11, and 4-perfluoroacylisoxazoles 13 are obtained in high chemical yields and complete site and regioselectivity through the reaction of β-perfluoroalkyl-β-dicarbonyls 2 with hydrazonyl halides 1 and halooximes 8 in the presence of bases. β-Perfluoroalkyl-β-dicarbonyls 2 are shown to be convenient precursors of 5-perfluoroalkypyrazoles 6, 5-perfluoroalkylisoxazoles 11, and 4-perfluoroacylisoxazoles 13.
1994
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11311/655557
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