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Reductive silylation of gem-difluorinated phosphonium salts
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01.01.2018 |
Tsymbal A.
Levin V.
Struchkova M.
Kokorekin V.
Korlyukov A.
Dilman A.
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Journal of Fluorine Chemistry |
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4 |
Ссылка
© 2017 Elsevier B.V. gem-Difluorinated phosphonium salts, generated from aldehydes and difluorinated phosphobetaine reagent, were converted into corresponding silicon reagents. The reductive silylation of carbon-phosphorus bond is carried out using a combination of magnesium and chlorotrimethylsilane in dimethylformamide. For a model difluoroined phosphonium salt, X-ray structure and reduction potential are provided.
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