Photoredox-catalyzed protecting-group-free C -glycosylation with glycosyl sulfinate via the Giese reaction

-Glycoside analogs of naturally occurring glycoconjugates are useful tools for chemical biology studies, but their synthesis usually requires protection of the hydroxyl groups of the glycosyl donors. Here we report protecting-group-free and photoredox-catalyzed -glycosylation with glycosyl sulfinate...

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Published in:Chemical communications (Cambridge, England) England), 2023-07, Vol.59 (55), p.8564-8567
Main Authors: Miura, Taishi, Yoritate, Makoto, Hirai, Go
Format: Article
Language:English
Subjects:
Chemical synthesis
Hydroxyl groups
Photoredox catalysis
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description -Glycoside analogs of naturally occurring glycoconjugates are useful tools for chemical biology studies, but their synthesis usually requires protection of the hydroxyl groups of the glycosyl donors. Here we report protecting-group-free and photoredox-catalyzed -glycosylation with glycosyl sulfinates and Michael acceptors the Giese radical addition.
doi_str_mv 10.1039/d3cc02361c
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source Royal Society of Chemistry:Jisc Collections:Royal Society of Chemistry Read and Publish 2022-2024 (reading list)
subjects Chemical synthesis
Hydroxyl groups
Photoredox catalysis
title Photoredox-catalyzed protecting-group-free C -glycosylation with glycosyl sulfinate via the Giese reaction
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