92517-03-8

Upstream product

• 89539-39-9 2,3,5,6-tetra-O-benzyl-α/β-D-galactofuranose 
• 92619-92-6 3,4,5,7-tetra-O-benzyl-1,2-dideoxy-D-manno-hept-1-enitol 
• 4132-28-9 2,3,4,6-tetra-O-benzyl-D-mannopyranose 
• 3879-79-6 (2R,3R,4S,5S,6S)-3,4,5-tris(benzyloxy)-2-((benzyloxy)methyl)-6-methoxytetrahydro-2H-pyran 
• 617-04-9 (2R,3S,4S,5S,6S)-2-(hydroxymethyl)-6-methoxytetrahydro-2H-pyran-3,4,5-triol 
• 100-39-0 benzyl bromide 
• 116444-14-5 3,4,6,7-tetra-O-benzyl-1,2-dideoxy-d-galacto-hept-1-enitol 

Downstream Products

• 92619-96-0 diethyl (((2S,3S,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-yl)methyl)phosphonate 

Relevant academic research and scientific papers

CARBOHYDRATE PHOSPHONATE DERIVATIVES AS MODULATORS OF GLYCOSYLATION

Compounds of Formula (I) are useful as modulators of glycosylation. Compounds of Formula (I) have the following structure: (I) and the definitions of the other variables are provided herein.

SYNTHESIS OF C-GLYCOSYL COMPOUNDS BY THE WITTIG IODOCYCLIZATION PROCEDURE. DIFFERENCES FROM MERCURIOCYCLIZATION

Various sugars were C-glycosylated by treatment with methylenetriphenylphosphorane and subsequent iodocyclization of the resulting hept- and hex-enitols.In all cases, a C-glycofuranosyl compound was obtained, except for 3,4,5,7-tetra-O-benzyl-1,2-dideoxy-