65434-49-3Relevant articles and documents
Environment friendly chemoselective deprotection of acetonides and cleavage of acetals and ketals in aqueous medium without using any catalyst or organic solvent
Mukherjee,Sengupta,Roy
, p. 1493 - 1496 (2014/04/03)
Highly chemoselective environment friendly deprotection of acetonides and cleavage of acetals and ketones has been achieved by heating in aqueous medium without using any catalyst and organic solvent. Indian Academy of Sciences.
First synthesis of 5,6-branched galacto-hexasaccharide, the dimer of the trisaccharide repeating unit of the cell-wall galactans of Bifidobacterium catenulatum YIT 4016
Zhang, Guohua,Fu, Mingkun,Ning, Jun
, p. 733 - 738 (2007/10/03)
α-d-Galactopyranosyl-(1→6)-[β-d-galactofuranosyl-(1→5) ]-β-d-galactofuranosyl-(1→6)-β-d-galactofuranosyl-(1→5) -[α-d-galactopyranosyl-(1→6)]-β-d-galactofuranose, the dimer of the trisaccharide repeating unit of the cell-wall galactans of Bifidobacterium c
A Simple and Facile Chemo- and Regioselective Deprotection of Acetonides Using Silica Supported Sodium Hydrogen Sulfate as a Heterogeneous Catalyst
Mahender,Ramu,Ramesh,Das, Biswanath
, p. 734 - 735 (2007/10/03)
Silica supported sodium hydrogen sulfate (NaHSO4·SiO 2) has been found to be an efficient heterogeneous catalyst for chemo- and regioselective deprotection of acetonides at room temperature to produce the corresponding diols in excellent yields.