
Bulletin of the Chemical Society of Japan p. 805 - 819 (1999)
Update date:2022-07-29
Topics:
Furuta, Satoru
Kuroboshi, Manabu
Hiyama, Tamejiro
Trifluoromethyl-substituted aromatic compounds were easily synthesized by the oxidative desulfurization-fluorination reaction of readily accessible methyl arenecarbodithioates using [n-Bu4N]H2F3 and 1,3-dibromo-5,5- dimethylhydantoin (DBH) under extremely mild conditions. Use of N- bromosuccinimide or N-iodosuccinimide instead of DBH afforded difluoro(methylthio)methyl-substituted aromatics. In a similar way, 3,3,3- trifluoropropenyl-substituted aromatic compounds were readily prepared from the corresponding α,β-unsaturated carbodithioates.
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Doi:10.1039/a808061e
(1999)Doi:10.1023/A:1021293532046
(2002)Doi:10.1016/S0223-5234(99)80047-6
(1999)Doi:10.1016/S0040-4020(99)00148-9
(1999)Doi:10.1021/co500181b
(2015)Doi:10.1021/ja01025a069
(1968)