
Journal of Fluorine Chemistry p. 149 - 153 (1997)
Update date:2022-08-17
Topics:
Ould Amanetoullah
Chaabouni
Baklouti
F-alkyl α-hydroxy acids and F-alkyl α-bromo acids were prepared respectively by the nitric acid ring-opening oxidative reaction of F-alkyl oxiranes, and oxidation by chromic acid of F-alkyl bromohydrins. The synthesized acids were converted to the corresponding methyl esters which may prove to be useful in the synthesis of F-alkylated heterocycles.
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