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• W4320032755 abstract "A metal-free and oxidant-free electrochemically enabled strategy for C-3 formylation of imidazopyridines using trimethylamine as a one-carbon source has been established. This conversion has high functional group compatibility under mild conditions and ensures late-stage functionalization of pharmaceutical molecules. Furthermore, unexpected hexafluoroisopropoxylation products have been observed in some cases. Mechanistic studies using cyclic voltammetry and control experiments reveal the key intermediate of the formylation process." @default.
• W4320032755 created "2023-02-12" @default.
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• W4320032755 date "2023-03-01" @default.
• W4320032755 modified "2023-10-10" @default.
• W4320032755 title "Electrochemically Enabled Direct C3‐Formylation of Imidazopyridines with Me₃N as a Carbonyl Source" @default.
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• W4320032755 doi "https://doi.org/10.1002/asia.202300001" @default.
• W4320032755 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36772840" @default.
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