A heterogenized iridium catalyst was employed to perform photoredox catalysis for a collection of mechanistically orthogonal reactions using very low quantities of iridium (0.01-0.1 mol %).
View Article and Find Full Text PDFA visible-light mediated alkoxy radical generation is described, which allows for a structurally divergent oxidative C(sp)-H bond functionalization. This protocol employs a photoredox/iron dual catalysis allowing for an unprecedented chemoselective single-step transformation of alcohol derivatives giving access to two valuable sets of products, tetrahydrofurans and γ-bromoketones, under one set of conditions. Addition of iron, by slow corrosion of a needle, provides superior reaction efficiency as compared to various iron(III) complexes.
View Article and Find Full Text PDFA new method employing iron(III) acetylacetonate along with visible light is described to effect oxidative ring opening of cyclic ethers and acetals with unparalleled efficiency. The method allows for a photocatalytic radical chemistry approach to functionalize relatively inert cyclic ethers into useful synthetic intermediates. The methodology sheds further light on the use of underexplored iron complexes in visible-light photochemical contexts and illustrates that simple Fe(III) complexes can initiate redox processes from LMCT excited states.
View Article and Find Full Text PDFA very efficient one-pot procedure for the direct oxidation of aldehydes to esters mediated by visible-light is presented. Utilizing a combination of indium triflate and N-bromosuccinimide, NBS, with either ortho-esters or alcohols provided rapid access to a variety of esters. Certain substrates convert fully within a few seconds, other more challenging tert-butyl esters were formed in good yield after no more than 4 h.
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