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- W4360994621 abstract "Abstract We describe an operationally simple and user‐friendly protocol that allows the site‐selective hydrogenation and deuteration of di‐, tri‐ and tetrasubstituted benzylic olefins by electroreduction while other groups prone to hydrogenation are present. The radical anionic intermediates react with the most inexpensive hydrogen/deuterium source H 2 O/D 2 O. Our method overcomes many limitations that arise from previously reported electroreductive hydrogenations. The applicability of this reaction is demonstrated by a broad substrate scope (>50 examples) that focuses on functional group tolerance and sites that are affected by metal‐catalyzed hydrogenation (alkenes, alkynes, protecting groups)." @default.
- W4360994621 created "2023-03-30" @default.
- W4360994621 creator A5011418889 @default.
- W4360994621 creator A5079173916 @default.
- W4360994621 date "2023-04-21" @default.
- W4360994621 modified "2023-10-18" @default.
- W4360994621 title "Site‐selective Hydrogenation/Deuteration of Benzylic Olefins Enabled by Electroreduction Using Water" @default.
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- W4360994621 doi "https://doi.org/10.1002/chem.202300849" @default.
- W4360994621 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36972395" @default.
- W4360994621 hasPublicationYear "2023" @default.
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