Fluorinated stannanes : Part 2. The stereospecific synthesis of fluorinated stannanes via a Barbier-type reaction between fluorinated halides and tributyltin chloride mediated by zinc or cadmium |
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Authors: | Donald J. Burton Vinod Jairaj |
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Affiliation: | Department of Chemistry, The University of Iowa, Iowa City, IA 52242, USA |
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Abstract: | Fluorinated stannanes are valuable synthons in synthetic organofluorine chemistry. Fluorinated vinyl, alkyl and aryl halides reacted efficiently with tri-n-butyltin chloride in the presence of zinc or cadmium to yield the corresponding stannanes in good yields. In some cases, yield of the stannanes showed a dramatic improvement over the transmetalation method. In all other cases, comparable yields were obtained. |
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Keywords: | Fluorinated vinyl Aryl and alkyl stannanes Tri-n-butyltin chloride Barbier reactions 119Sn NMR spectra |
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