Glycosyl-Radical-Based Synthesis of C‑Alkyl Glycosides via Photomediated Defluorinative gem-Difluoroallylation

We have developed a stereoselective, glycosyl radical-based method for the synthesis of C-alkyl glycosides via a photomediated defluorinative gem-difluoroallylation reaction. We demonstrate for the first time that glycosyl radicals, generated from glycosyl bromides, can readily participate in a phot...

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Veröffentlicht in:Organic letters 2021-11, Vol.23 (22), p.8899-8904
Hauptverfasser: Li, Cai-Yi, Ma, Yue, Lei, Zhi-Wei, Hu, Xiang-Guo
Format: Artikel
Sprache:eng
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Zusammenfassung:We have developed a stereoselective, glycosyl radical-based method for the synthesis of C-alkyl glycosides via a photomediated defluorinative gem-difluoroallylation reaction. We demonstrate for the first time that glycosyl radicals, generated from glycosyl bromides, can readily participate in a photomediated radical polar crossover process, affording a diverse array of gem-difluoroalkene containing C-glycosides. Notable features of this method include scalability, mild conditions, broad substrate scope, and suitability for the late-stage modification of complex molecules.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.1c03390