134275-41-5

Upstream product

• 582-52-5 1,2:5,6-Di-O-isopropylidene-β-D-altrofuranose 
• 134275-38-0 1,2:5,6-di-O-isopropylidene-3-O-benzyl-β-D-altrofuranose 
• 100-39-0 benzyl bromide 
• 134275-39-1 3-O-benzyl-1,2-O-isopropylidene-β-D-altrofuranose 
• 98-59-9 p-toluenesulfonyl chloride 
• 591727-19-4 1-2,5-6 di-O-isopropylidene 3-O-benzyl α(D)gluco-pentoaldofuranose 
• 908142-25-6 1-2 O-isopropylidene 3-O-benzyl α(D)gluco-pentoaldofuranose 
• 350255-13-9 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 

Downstream Products

• 37073-74-8 3-O-benzyl-1,2-O-isopropylidene-6-O-tosyl-β-D-arabino-hexofuranos-5-ulose 
• 134275-44-8 (5R and 5S)-5,6-anhydro-1,2-O-isopropylidene-5-<(R and S)-(methoxy)phenylphosphinyl>-3-O-benzyl-β-D-arabino-hexofuranoses 
• 134275-46-0 (5R and 5S)-5,6-dideoxy-1,2-O-isopropylidene-5-<(R and S)-(methoxy)phenylphosphinyl>-3-O-benzyl-β-D-arabino-hexofuranoses 
• 134275-48-2 (5R and 5S)-5,6-dideoxy-1,2-O-isopropylidene-5-<(R and S)-(methoxy)phenylphosphinyl>-β-D-arabino-hexofuranoses 
• 83167-68-4 (3aS,5S,6S,6aS)-2,2-Dimethyl-5-(1-phenylphosphinoyl-ethyl)-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol 

Relevant academic research and scientific papers

Metal free synthesis of morpholine fused [5,1-c] triazolyl glycoconjugates via glycosyl azido alcohols

A series of diverse glycosyl 1,2-azido alcohols, obtained from readily available carbohydrates, were converted to structurally varied rare and novel sugar derived morpholine fused [5,1-c]-triazoles via a one-pot strategy. After incorporating a propargyl functionality at the hydroxyl group of the sugar derived 1,2-azido alcohols, the resulting in situ generated azido-alkyne affords numerous C- and O-glycosyl bicyclic ring systems with medicinal value via a metal free cycloaddition reaction. The structures of all the developed molecules have been elucidated using 1H NMR, 13C NMR, IR and MS spectroscopy.

Synthesis of 5,6-Dideoxy-5-phenylphosphinyl-L-galactopyranoses. The P-in-Ring Sugar Analogs of L-Fucose

1,2-O-Isopropylidene-3-O-methyl-6-O-tosyl-β-D-arabino-hexofuranos-5-ulose (9a) and its 3-O-benzyl congener (9b) were prepared from 1,2:5,6-di-O-isopropylidene-β-D-altrofuranose in 4 steps.Addition of methyl phenylphosphinate to 9a and 9b in the presence o