1992
DOI: 10.1002/hc.520030311
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Preparation of α,α‐difluoromethylene functionalized sulfones

Abstract: Sulfination

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Cited by 12 publications
(1 citation statement)
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“…By way of example, Yagupolskii et al obtained ethyl 2,2-difluoro-2-(phenylthio)acetates by nucelophilic substitution of ethyl difluoroiodoacetate with thiophenols in the presence of a base [12b]. Also ethyl bromodifluoroacetate was successfully applied to synthesize the latter compound [14]. Furthermore, the Na 2 S 2 O 4 mediated addition of difluoroiodomethylsulfanyl benzene to alkenes and alkynes gave 2,2-difluoro-4-iodoalkyl aryl sulfides [15].…”
Section: Introductionmentioning
confidence: 98%
“…By way of example, Yagupolskii et al obtained ethyl 2,2-difluoro-2-(phenylthio)acetates by nucelophilic substitution of ethyl difluoroiodoacetate with thiophenols in the presence of a base [12b]. Also ethyl bromodifluoroacetate was successfully applied to synthesize the latter compound [14]. Furthermore, the Na 2 S 2 O 4 mediated addition of difluoroiodomethylsulfanyl benzene to alkenes and alkynes gave 2,2-difluoro-4-iodoalkyl aryl sulfides [15].…”
Section: Introductionmentioning
confidence: 98%