Electro-mediated photoredox catalysis for selective C(sp3)-O cleavages of phosphinates to carbanions
Tian, Xianhai and Karl, Tobias and Reiter, Sebastian and Yakubov, Shahboz and de Vivie-Riedle, Regina and Koenig, Burkhard and Barham, Joshua (2021) Electro-mediated photoredox catalysis for selective C(sp3)-O cleavages of phosphinates to carbanions. Other. ChemRxiv. (https://doi.org/10.26434/chemrxiv.14753523.v1)
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Abstract
We report a novel example of electro-mediated photoredox catalysis (e-PRC) in the reductive cleavage of C(sp3)-O bonds of phosphinates to alkyl carbanions. As well as deoxygenations, olefinations are reported which are E-selective and can be made Z-selective in a tandem reduction/photosensitization process where both steps are photoelectrochemically promoted. Spectroscopy, computation and catalyst structural variations reveal that our new naphthalene monoimide-type catalyst allows for a more intimate dispersive precomplexation of its radical anion form with the phosphinate substrate, facilitating a reactivity-determining C(sp3)-O cleavage. Surprisingly and in contrast to previously reported photoexcited radical anion chemistries, our conditions i) tolerate aryl chlorides/bromides and ii) do not give rise to Birch-type reductions.
ORCID iDs
Tian, Xianhai, Karl, Tobias, Reiter, Sebastian, Yakubov, Shahboz, de Vivie-Riedle, Regina, Koenig, Burkhard and Barham, Joshua
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Item type: Monograph(Other) ID code: 92165 Dates: DateEvent11 June 2021PublishedSubjects: Science > Chemistry Department: Faculty of Science > Pure and Applied Chemistry Depositing user: Pure Administrator Date deposited: 24 Feb 2025 16:09 Last modified: 24 Feb 2025 16:09 URI: https://strathprints.strath.ac.uk/id/eprint/92165