Halogenation of fluoroalkyl-substituted β-ketoesters
1984
1.
The bromination of fluoroalkyl-substituted β-ketoesters using bromine gives unstable α-bromo derivatives which undergo intermolecular rearrangement to yield the starting β-ketoesters and α,α-dibromo-β-ketoesters.
2.
An IR spectroscopic and dipole moment study showed that the z- and q-conformers relative to the ester C=0 bond are equally probable for the fluoroalkyl-substituted β-ketoesters.
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