A Practical Source of Chlorodifluoromethyl Radicals. Convergent Routes to gem-Difluoroalkenes and -dienes and (2,2-Difluoroethyl)-indoles, -azaindoles, and -naphthols.

Pierre Salomon 1, * Samir Zard 1, *
* Corresponding author
1 DCSO - Laboratoire de synthèse organique
Abstract : The preparation of O-octadecyl-S-chlorodifluoromethyl xanthate from chlorodifluoroacetic acid and its use as a convenient source of chlordifluoromethyl radicals is described. This reagent may be used to access gem-difluoroalkenes and -dienes, as well as (2,2-difluoroethyl)indolines, -indoles, and -naphthols.
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Journal articles
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Submitted on : Thursday, July 3, 2014 - 2:06:24 PM
Last modification on : Thursday, February 7, 2019 - 5:16:41 PM

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CNRS | PARISTECH | X | X-DCSO | INC-CNRS | X-DEP-CHIM

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Pierre Salomon, Samir Zard. A Practical Source of Chlorodifluoromethyl Radicals. Convergent Routes to gem-Difluoroalkenes and -dienes and (2,2-Difluoroethyl)-indoles, -azaindoles, and -naphthols.. Organic Letters, American Chemical Society, 2014, 16 (11), pp.2926-2929. ⟨10.1021/ol501063a⟩. ⟨hal-01017932⟩

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