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A mild, efficient, and selective procedure for transprotection of acetonides to acetates catalyzed with HClO4–SiO2

Authors :
Liu, Hai-Xia
Wu, Qin-Pei
Shu, Yi-Nan
Chen, Xi
Xi, Xiao-Dong
Du, Ti-Jian
Zhang, Qing-Shan
Source :
Carbohydrate Research. Nov2009, Vol. 344 Issue 17, p2342-2348. 7p.
Publication Year :
2009

Abstract

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. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
00086215
Volume :
344
Issue :
17
Database :
Academic Search Index
Journal :
Carbohydrate Research
Publication Type :
Academic Journal
Accession number :
44941740
Full Text :
https://doi.org/10.1016/j.carres.2009.08.035