Hypervalent Iodine-Mediated
Fluorination of Styrene
Derivatives: Stoichiometric and Catalytic Transformation to 2,2-Difluoroethylarenes
Posted on 2015-11-06 - 00:00
Fluorination of styrene derivatives
with a reagent system composed
of μ-oxo-bis[trifluoroacetato(phenyl)iodine] and a pyridine·HF
complex gave the corresponding (2,2-difluoroethyl)arenes in good yields.
Similarly, the reagent of PhI(OCOCF3)2 and the
pyridine·HF complex acted as a fluorinating agent for styrene
derivatives. The fluorination of styrene derivatives with the pyridine·HF
complex underwent under catalytic conditions using 4-iodotoluene as
a catalyst and m-CPBA as a terminal oxidant.
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Kitamura, Tsugio; Muta, Kensuke; Oyamada, Juzo (2016). Hypervalent Iodine-Mediated
Fluorination of Styrene
Derivatives: Stoichiometric and Catalytic Transformation to 2,2-Difluoroethylarenes. ACS Publications. Collection. https://doi.org/10.1021/acs.joc.5b01929