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Synlett 2016; 27(05): 749-753
DOI: 10.1055/s-0035-1561284
DOI: 10.1055/s-0035-1561284
cluster
Visible-Light-Activated Enantioselective Perfluoroalkylation with a Chiral Iridium Photoredox Catalyst
Weitere Informationen
Publikationsverlauf
Received: 31. Oktober 2015
Accepted: 18. November 2015
Publikationsdatum:
23. Dezember 2015 (online)

Abstract
A visible-light-activated enantioselective radical perfluoroalkylation of 2-acyl imidazoles with perfluoroalkyl iodides (CF3I, C3F7I, C4F9I, C6F13I, C8F17I and C10F21I) and perfluorobenzyl iodide at the α-position of the carbonyl group is reported. Enantioselectivities with up to >99.5% ee are achieved. The process uses a dual-function chiral Lewis acid/photoredox catalyst at loadings of 2–4 mol% and constitutes a redox-neutral, electron-catalyzed reaction that proceeds via intermediate perfluoroalkyl radicals.
Key words
photoredox catalysis - asymmetric catalysis - visible light - perfluoroalkylation - radical reaction - electron catalysisSupporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0035-1561284.
- Supporting Information
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For reviews on asymmetric catalysis through visible-light activation, see:
For reviews on photoredox catalysis, see:
For selected examples, see:
For perfluoroalkylations through photoredox chemistry, see: