1029039-49-3

Upstream product

• 3282-30-2 pivaloyl chloride 
• 260963-53-9 2,2-Dimethyl-propionic acid (2R,3R,5R)-3-benzyloxy-5-(1,3-dioxo-1,3-dihydro-isoindol-2-ylsulfanyl)-4,6-dioxo-tetrahydro-pyran-2-ylmethyl ester 
• 260963-68-6 2,2-Dimethyl-propionic acid (2R,3S,5R)-3-benzyloxy-5-(1,3-dioxo-1,3-dihydro-isoindol-2-ylsulfanyl)-4,6-dioxo-tetrahydro-pyran-2-ylmethyl ester 
• 629652-14-8 4-O-benzyl-2-deoxy-6-O-pivaloyl-α,β-D-glucopyranose 
• 629652-15-9 4-O-benzyl-2-deoxy-6-O-pivaloyl-α,β-D-galactopyranose 
• 260963-51-7 4-O-benzyl-2-deoxy-1-oxo-6-O-pivaloyl-D-(+)-glucopyranose 
• 260963-64-2 4-O-benzyl-2-deoxy-1-oxo-6-O-pivaloyl-D-(+)-galactopyranose 
• 260963-50-6 4-O-benzyl-2-deoxy-1,3-dioxo-6-O-pivaloyl-D-(+)-glucopyranose 
• 260963-66-4 4-O-benzyl-2-deoxy-1,3-dioxo-6-O-pivaloyl-D-galactopyranose 
• 260963-48-2 4-O-benzyl-6-O-pivaloyl-D-(+)-glucal 
• 260963-60-8 4-O-benzyl-6-O-pivaloyl-D-(-)-galactal 
• 157380-76-2 4-O-benzyl-D-(-)-galactal 
• 13265-84-4 D-glucal 
• 21193-75-9 D-galactal 

Relevant academic research and scientific papers

A new procedure for the preparation of β-keto-δ-lactones from sugars and their transformation into glycosyl acceptors in disaccharides synthesis

(matrix presented) Glycals are effective starting materials for the synthesis of enantiopure β-ketone-δ-lactones. They are easily transformed, through a two-step, one-pot reaction, into the corresponding α,α′-dioxothiones which in turn can be quantitative