2004
DOI: 10.1016/j.jfluchem.2004.01.016
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Reductive dimerization of dithianylium salts and fluorodesulfuration: a new synthetic approach to tetrafluoroethylene substructures

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Cited by 9 publications
(1 citation statement)
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“…Likewise, reductive dimerization of aromatic and perfluoroaliphatic dithianylium ions 126 can be accomplished in higher yields (47-96 %) and in a more convenient way by using TDAE instead of zinc. [104] Species 127 are important precursors of liquid-crystal building blocks. It is noteworthy that the electron transfer proceeds here between TDAE and a C=S + bond (instead of a CÀX bond).…”
Section: Miscellaneous Reactionsmentioning
confidence: 99%
“…Likewise, reductive dimerization of aromatic and perfluoroaliphatic dithianylium ions 126 can be accomplished in higher yields (47-96 %) and in a more convenient way by using TDAE instead of zinc. [104] Species 127 are important precursors of liquid-crystal building blocks. It is noteworthy that the electron transfer proceeds here between TDAE and a C=S + bond (instead of a CÀX bond).…”
Section: Miscellaneous Reactionsmentioning
confidence: 99%