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Merck

Trifluoromethylation of allylsilanes under photoredox catalysis.

Organic letters (2013-03-08)
Satoshi Mizuta, Keary M Engle, Stefan Verhoog, Oscar Galicia-López, Miriam O'Duill, Maurice Médebielle, Katherine Wheelhouse, Gerasimos Rassias, Amber L Thompson, Véronique Gouverneur
要旨

A new catalytic method to access allylic secondary CF3 products is described. These reactions use the visible light excited Ru(bpy)3Cl2·6H2O catalyst and the Togni or Umemoto reagent as the CF3 source. The photoredox catalytic manifold delivers enantioenriched allylic trifluoromethylated products not accessible under Cu(I) catalysis.

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Sigma-Aldrich
塩化銅(I), reagent grade, 97%
Sigma-Aldrich
塩化銅(I), ReagentPlus®, purified, ≥99%
Sigma-Aldrich
塩化銅(I), ≥99.995% trace metals basis
Sigma-Aldrich
塩化銅(I), AnhydroBeads, ≥99.99% trace metals basis
Sigma-Aldrich
塩化銅(I), JIS special grade, ≥95.0%