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Visible‐Light‐Mediated Photocatalytic Difunctionalization of Olefins by Radical Acylarylation and Tandem Acylation/Semipinacol Rearrangement
Authors:Dr. Giulia Bergonzini  Dr. Carlo Cassani  Haldor Lorimer‐Olsson  Johanna Hörberg  Dr. Carl‐Johan Wallentin
Affiliation:Department of Chemistry and Molecular Biology, Gothenburg University, Gothenburg, Sweden
Abstract:A novel method for the mild photoredox‐mediated tandem radical acylarylation and tandem acylation/semipinacol rearrangement has been developed. The synthesis of highly functionalized ketones bearing all‐carbon α‐ or β‐quaternary centers has been achieved using easily available symmetric aromatic carboxylic anhydrides as the acyl radical source. The method allows for a straightforward introduction of the keto functionality and concomitant construction of molecular complexity in a single operation.
Keywords:acylation  cyclization  oxindole  photoredox catalysis  synthetic methods
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