869795-79-9Relevant academic research and scientific papers
A short and simple synthesis of branched mannooligosaccharides with [1-13C]-labelled terminal mannose units
Ivlev,Backinowsky,Abronina,Kononov,Kochetkov
, p. 275 - 286 (2007/10/03)
Mannosylation with 2,3,4,6-tetra-O-benzoyl-α-D-[1- 13C]mannopyranosyl bromide as a glycosyl donor has been used for the synthesis of 3,6-branched mannotri- and -pentaoside bearing labelled terminal mannopyranose units. Methyl 2,4-di-O-benzoyl-α
An easy access to a 3,6-branched mannopentaoside bearing one terminal [1-13C]-labeled D-mannopyranose residue1
Abronina,Backinowsky,Grachev,Sedinkin,Malysheva
, p. 1287 - 1293 (2007/10/03)
Methyl 2,4-di-O-benzoyl-α-D-mannopyranoside was used as a key intermediate in the synthesis of 3,6-branched mannopentaoside bearing one terminal D-[1-13C]mannopyranose residue, viz., methyl 6-O-[3,6-di-O-(α-D-mannopyranosyl)-α-D-mannopyranosyl)
