50820-75-2Relevant articles and documents
A 2-silylethanol-based anomeric linker for carbohydrates; transformation into 1-0-acyl derivatives
Wallberg, Andreas,Weigelt, Dirk,Falk, Niklas,Magnusson, Goeran
, p. 4285 - 4286 (1997)
The novel linker 4 was synthesized in three steps from hex-5-enyldimethylchlorosilane and glycosylated with 2,3,4,6-tetra-O-benzoyl-α-D-galactopyran trichloroacetimidate to give the corresponding linker β-glycoside 5 (77%). Treatment of 5 with acetic anhydride and BF3·OEt2 gave 1-O-acetyl-2,3,4,6-tetra-O-benzonyl-β-D-galactose (~90%), devoid of the α-anomer.
SYNTHESIS OF DERIVATIVES OF 2-AMINO-2-DEOXY-4-O-(α- AND β-D-GALACTOPYRANOSYL)-D-GLUCOSE
Nifant'Ev, Nikolay E.,Backinowsky, Leon V.,Kochetkov, Nikolay K.
, p. 61 - 72 (2007/10/02)
Galactosylation of methyl 6-O-acetyl-3-O-benzoyl-2-deoxy-2-phthalimido-β-D-glucopyranoside (5) and its trityl ether 9 with 2,3,4,6-tetra-O-benzoyl-α-D-galactopyranosyl bromide (8), 1-O-acetyl-2,3,4,6-tetra-O-benzoyl-β-D-galactopyranose (13), 3,4,6-tri-O-b