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Palladium-Catalyzed One-Pot Stereospecific Synthesis of 2-Deoxy Aryl C-Glycosides from Glycals and Anilines in the Presence of tert-Butyl Nitrite

dc.contributor.authorSingh A.K.; Venkatesh R.; Kandasamy J.
dc.date.accessioned2025-05-24T09:40:17Z
dc.description.abstractThe palladium-catalyzed one-pot synthesis of 2,3-deoxy-3-keto aryl C-glycosides is achieved from glycals and anilines in the presence of tert-butyl nitrite and aqueous HBF 4 under mild conditions. This one-pot method stereospecifically provides α-and β-Aryl glycosides (≥19:1 by NMR) in good yields at room temperature. The configuration at the C-3 position in the glycal determines the anomeric selectivity (i.e., α or β) of the desired products. © 2019. Thieme. All rights reserved.
dc.identifier.doihttps://doi.org/10.1055/s-0037-1611916
dc.identifier.urihttp://172.23.0.11:4000/handle/123456789/19017
dc.relation.ispartofseriesSynthesis (Germany)
dc.titlePalladium-Catalyzed One-Pot Stereospecific Synthesis of 2-Deoxy Aryl C-Glycosides from Glycals and Anilines in the Presence of tert-Butyl Nitrite

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