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
Pages
7
From page
2342
To page
2348
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
Serial Year
2009
Journal title
Carbohydrate Research
Record number
966593
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