135129-62-3Relevant academic research and scientific papers
α-Fucosylation by 2,3,4-tri-O-benzoyl-α-L-fucopyranosyl bromide under Helferich conditions
Nifant'ev, Nikolay E.,Amochaeva, Vera Y.,Shashkov, Alexander S.,Kochetkov, Nikolay K.
, p. 77 - 90 (1993)
Glycosylation of various carbohydrate mono- and di-hydroxy derivatives with 2,3,4-tri-O-benzoyl-α-L-fucopyranosyl bromide under Helferich conditions is stereoselective for acceptors that contain an axial hydroxyl group and/or neighboring acyloxy, phthalimido, or bulky monosaccharide substitutents.
Studies on the conformational flexibility of α-l-rhamnose-containing oligosaccharides using 13C-site-specific labeling, NMR spectroscopy and molecular simulations: Implications for the three-dimensional structure of bacterial rhamnan polysaccha
Jonsson, K. Hanna M.,Saewen, Elin,Widmalm, Goeran
experimental part, p. 2453 - 2463 (2012/04/23)
Bacterial polysaccharides are comprised of a variety of monosaccharides, l-rhamnose (6-deoxy-l-mannose) being one of them. This sugar is often part of α-(1 → 2)- and/or α-(1 → 3)-linkages and we have therefore studied the disaccharide α-l-Rhap-(1 → 2)-α-l
Synthesis of di-O-glycosyl derivatives of methyl α-L-rhamnopyranoside
Nifant'ev, Nikolay E.,Lipkind, Grigory M.,Shashkov, Alexander S.,Kochetkov, Nikolay K.
, p. 109 - 128 (2007/10/02)
The syntheses are described of 2,3-di-O-glycosyl derivatives (1-12) of methyl α-L-rhamnopyranoside where the glycosyl moieties are variously α-L-fucopyranose, β-L-fucopyranose, β-D-glucopyranose, α-D-mannopyranose, and α-L-rhamnopyranose.The syntheses inv
