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Electrochemical Benzylic C(sp(3))–H Acyloxylation

[Image: see text] The development of sustainable C(sp(3))–H functionalization methods is of great interest to the pharmaceutical and agrochemical industries. Anodic oxidation is an efficient means of producing benzylic cations that can undergo subsequent in situ nucleophilic attack to afford functio...

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Detalles Bibliográficos
Autores principales: Atkins, Alexander P., Rowett, Albert C., Heard, David M., Tate, Joseph A., Lennox, Alastair J. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9315976/
https://www.ncbi.nlm.nih.gov/pubmed/35829756
http://dx.doi.org/10.1021/acs.orglett.2c01930
Descripción
Sumario:[Image: see text] The development of sustainable C(sp(3))–H functionalization methods is of great interest to the pharmaceutical and agrochemical industries. Anodic oxidation is an efficient means of producing benzylic cations that can undergo subsequent in situ nucleophilic attack to afford functionalized benzylic products. Herein, we demonstrate the suitability of carboxylic acids as nucleophiles to yield benzylic esters. This method employs a series of secondary benzylic substrates and functionalized carboxylic acids and is demonstrated on a gram scale in flow.