135129-62-3Relevant articles and documents
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.
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