Title of article
(E)-1,2-Difluoro-1-iodo-2-trialkylsilanes—A useful synthon for the addition of the [IFCCF] unit to activated electrophiles
Author/Authors
He، نويسنده , , Ya-Bo and Nguyen، نويسنده , , Ba V. and Burton، نويسنده , , Donald J.، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2011
Pages
5
From page
940
To page
944
Abstract
Fluoride ion catalyzed reaction of (E)-IFCCFSiR3 with activated aromatic aldehydes and ketones and activated perfluoroaromatics, such as pentafluoropyridine and perfluorotoluenes, transfers the [IFCCF] unit to the activated electrophiles to stereospecifically provide (E)-1,2-difluoro-1-iodosubstituted derivatives. Aluminum chloride catalyzed reaction of (E)-1,2-difluoro-1-iodo-2-trialkylsilanes with alkyl or aryl acyl halides gives the corresponding (E)-1,2-difluoro-1-iodoketones stereospecifically in excellent yield. The vinyl iodide product formed via this methodology could be coupled (with Pd(0)) catalysis to provide an entry to a polyfunctionalized derivative.
Keywords
AlCl3 catalysis , Perfluoroaromatics , Fluoride ion mediated reactions , Fluorinated vinylsilanes
Journal title
Journal of Fluorine Chemistry
Serial Year
2011
Journal title
Journal of Fluorine Chemistry
Record number
1611417
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