Electrochemical quinuclidine-mediated Minisci-type acylation of N-heterocycles with aldehydes

The electro-generation of acyl radicals from both aromatic and aliphatic aldehydes remains an unmet challenge. We provide a solution to this challenge by merging electro-oxidation and a quinuclidine-mediated hydrogen atom transfer strategy. The generation of acyl radicals at decreased applied potent...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2024-06, Vol.6 (48), p.6174-6177
Hauptverfasser: Li, Yongmei, Sun, Liangbo, Huang, Shengyang, Xu, Kun, Zeng, Cheng-Chu
Format: Artikel
Sprache:eng
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Zusammenfassung:The electro-generation of acyl radicals from both aromatic and aliphatic aldehydes remains an unmet challenge. We provide a solution to this challenge by merging electro-oxidation and a quinuclidine-mediated hydrogen atom transfer strategy. The generation of acyl radicals at decreased applied potentials compared to that of formyl oxidation exhibits excellent functional group compatibility. The electro-generation of acyl radicals from both aromatic and aliphatic aldehydes is a synthetic challenge. We addressed this challenge by merging electro-oxidation and a quinuclidine-mediated HAT strategy.
ISSN:1359-7345
1364-548X
DOI:10.1039/d4cc00800f