128848-36-2

Upstream product

• 72074-91-0 3-O-acetyl-1,5-anhydro-4,6-O-benzylidene-2-deoxy-D-ribo-hex-1-enitol 
• 4064-06-6 1,2:3,4-di-O-isopropylidene-α-D-galactopyranose 

Downstream Products

• 128848-43-1 (3aR,5R,5aS,8aS,8bR)-2,2,7,7-Tetramethyl-5-((2R,4aR,6S,8aS)-2-phenyl-4,4a,6,8a-tetrahydro-pyrano[3,2-d][1,3]dioxin-6-yloxymethyl)-tetrahydro-bis[1,3]dioxolo[4,5-b;4',5'-d]pyran 
• 128848-37-3 1,2;3,4-di-O-isopropylidene-6-O-(2,3-anhydro-4,6-O-benzylidene-α-D-allopyranosyl)-α-D-galactopyranose 
• 128848-44-2 1,2;3,4-di-O-isopropylidene-6-O-(2,3-di-O-acetyl-4,6-O-benzylidene-α-D-mannopyranosyl)-α-D-galactopyranose 
• 128848-40-8 1,2;3,4-di-O-isopropylidene-6-O-(2-amino-2-deoxy-3-O-benzoyl-4,6-O-benzylidene-α-D-altropyranosyl)-α-D-galactopyranose 
• 263543-81-3 6-O-[4,6-O-benzylidene-α-D-mannopyranosyl]-1,2:3,4-di-O-isopropylidene-α-D-galactopyranoside 
• 532-32-1 sodium benzoate 

Relevant academic research and scientific papers

On the use of the haloetherification method to synthesize fully functionalized disaccharides

Synthetic routes to the fully functionalized α-linked disaccharides 19 21 and 25 are described starting from a common intermediate the iodo acetate 15. This substance was in turn prepared via a haloetherification reaction between the allal derivative 13 the galactose alcohol 14 and an "iodonium" equivalent.