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.author | Singh A.K.; Venkatesh R.; Kandasamy J. | |
| dc.date.accessioned | 2025-05-24T09:40:17Z | |
| dc.description.abstract | The 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.doi | https://doi.org/10.1055/s-0037-1611916 | |
| dc.identifier.uri | http://172.23.0.11:4000/handle/123456789/19017 | |
| dc.relation.ispartofseries | Synthesis (Germany) | |
| dc.title | Palladium-Catalyzed One-Pot Stereospecific Synthesis of 2-Deoxy Aryl C-Glycosides from Glycals and Anilines in the Presence of tert-Butyl Nitrite |