Glycosylation employing glycopyranosyl fluorides promoted by TiF4 under mild conditions
摘要:
Glycopyranosyl fluorides are shown as efficient glycosyl donors by glycosylation of appropriate aglycon structures under mild conditions with Lewis acid catalysis in anhydrous ether or acetonitrile. Further direct reaction sequences gave naturally occurring disaccharide derivatives of biological interest.
Glycosylation employing glycopyranosyl fluorides promoted by TiF<sub>4</sub> under mild conditions
作者:Joachim Thiem、Matthias Wiesner
DOI:10.1080/07328303.2020.1837151
日期:2020.10.12
Glycopyranosyl fluorides are shown as efficient glycosyl donors by glycosylation of appropriate aglycon structures under mild conditions with Lewis acid catalysis in anhydrous ether or acetonitrile. Further direct reaction sequences gave naturally occurring disaccharide derivatives of biological interest.