Fluoroselenenylation of α-diazoketones and α-diazoesters using a phenylselenenyl fluoride equivalent, generated in situ from phenylselenenyl bromide and AgF, followed by oxidation with hydrogen peroxide, provided α-fluoro-α,β-unsaturated ketones and ester, respectively, in moderate yields.
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Usuki et al. (1992) studied this question.
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