Radical C-Glycosylation Using Photoexcitable Unprotected Glycosyl Borate.
Chemistry
; 30(51): e202402256, 2024 Sep 11.
Article
in En
| MEDLINE
| ID: mdl-38980084
ABSTRACT
We have developed radical C-glycosylation using photoexcitable unprotected glycosyl borate. The direct excitation of glycosyl borate under visible light irradiation enabled the generation of anomeric radical without any photoredox catalysts. The inâ
situ generated anomeric radical was applicable to the radical addition such as Giese-type addition and Minisci-type reaction to introduce alkyl and heteroaryl groups at the anomeric position. In addition, the radical-radical coupling between the glycosyl borate and acyl imidazolide provided unprotected acyl C-glycosides.
Full text:
1
Database:
MEDLINE
Language:
En
Journal:
Chemistry
Journal subject:
QUIMICA
Year:
2024
Type:
Article
Affiliation country:
Japan