Title of article :
A mild, efficient, and selective procedure for transprotection of acetonides to acetates catalyzed with HClO4–SiO2 Original Research Article
Author/Authors :
Haixia Liu، نويسنده , , Qin-Pei Wu، نويسنده , , Yi-Nan Shu، نويسنده , , Xi Chen، نويسنده , , Xiao-Dong Xi، نويسنده , , Ti-Jian Du، نويسنده , , Qingshan Zhang، نويسنده ,
Issue Information :
دوهفته نامه با شماره پیاپی سال 2009
Abstract :
The transformation of acetonides into acetates is frequently required in synthetic chemistry. An efficient procedure for direct conversion of acetonides into acetates in the presence of HClO4–SiO2 under mild conditions was developed. The acetonides of primary hydroxy groups are directly converted to diacetates, and the anomeric acetonides of furanosides are stereoselectively transformed into the corresponding acetyl β-d-furanosides with a 2-acetoxyisopropyl group.
Keywords :
Acetals , Esterification , Esters , Protecting groups , Heterogeneous catalysis
Journal title :
Carbohydrate Research
Journal title :
Carbohydrate Research