Journal of the Chemical Society. Chemical communications p. 1065 - 1066 (1990)
Update date:2022-08-17
Topics:
Meio, Giuseppe V. De
Pinhey, John T.
Aryl-lead(IV) triacetates react at room temperature with BF3*Et2O to give the corresponding aryl fluoride in moderate to good yields; triarylboroxines, electron-rich aryltrimethylsilanes, and some arenes, which yield aryl-lead(IV) triacetates in acid catalysed reactions with lead tetra-acetate, may be converted directly into aryl fluorides when stirred with lead tetra-acetate in BF3*Et2O.
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