ChemInform Abstract: Catalytic Hydrotrifluoromethylation of Unactivated Alkenes
(2013)
Journal Article
Mizuta, S., Verhoog, S., Engle, K. M., Khotavivattana, T., O'Duill, M., Wheelhouse, K., …Gouverneur, V. (2013). ChemInform Abstract: Catalytic Hydrotrifluoromethylation of Unactivated Alkenes. ChemInform, 44(30), https://doi.org/10.1002/chin.201330058
Outputs (4)
Catalytic Decarboxylative Fluorination for the Synthesis of Tri- and Difluoromethyl Arenes (2013)
Journal Article
Mizuta, S., S. R. Stenhagen, I., O’Duill, M., Wolstenhulme, J., K. Kirjavainen, A., J. Forsback, S., …Gouverneur, V. (2013). Catalytic Decarboxylative Fluorination for the Synthesis of Tri- and Difluoromethyl Arenes. Organic Letters, 15(11), 2648-2651. https://doi.org/10.1021/ol4009377Treatment of readily available α,α-difluoro- and α-fluoroarylacetic acids with Selectfluor under Ag(I) catalysis led to decarboxylative fluorination. This operationally simple reaction gave access to tri- and difluoromethylarenes applying a late-stag... Read More about Catalytic Decarboxylative Fluorination for the Synthesis of Tri- and Difluoromethyl Arenes.
Trifluoromethylation of Allylsilanes under Photoredox Catalysis (2013)
Journal Article
Mizuta, S., Engle, K. M., Verhoog, S., Galicia-López, O., O’Duill, M., Médebielle, M., …Gouverneur, V. (2013). Trifluoromethylation of Allylsilanes under Photoredox Catalysis. Organic Letters, 15(6), 1250–1253. https://doi.org/10.1021/ol400184tA 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 enant... Read More about Trifluoromethylation of Allylsilanes under Photoredox Catalysis.
Catalytic Hydrotrifluoromethylation of Unactivated Alkenes (2013)
Journal Article
Mizuta, S., Verhoog, S., Engle, K. M., Khotavivattana, T., O’Duill, M., Wheelhouse, K., …Gouverneur, V. (2013). Catalytic Hydrotrifluoromethylation of Unactivated Alkenes. Journal of the American Chemical Society, 135(7), 2505–2508. https://doi.org/10.1021/ja401022xA visible-light-mediated hydrotrifluoromethylation of unactivated alkenes that uses the Umemoto reagent as the CF3 source and MeOH as the reductant is disclosed. This effective transformation operates at room temperature in the presence of 5 mol % Ru... Read More about Catalytic Hydrotrifluoromethylation of Unactivated Alkenes.