Journal of the Chemical Society. Chemical communications p. 1148 - 1150 (1992)
Update date:2022-08-04
Topics:
Usuki, Yoshinosuke
Iwaoka, Michio
Tomoda, Shuji
Fluoroselenylation of α-diazoketones and α-diazoesters using a phenylselenyl 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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