77340-95-5

Usage

Uses

Used in Organic Synthesis:
2,4-O-BENZYLIDENE-D-GLUCITOL is used as a chiral auxiliary for [assisting in the synthesis of chiral compounds] because of its ability to form stable complexes with a variety of chiral compounds.
Used in Pharmaceutical Industry:
2,4-O-BENZYLIDENE-D-GLUCITOL is used as a building block for [synthesis of complex organic molecules and production of enantiopure drug molecules] due to its unique structure and reactivity.

Upstream product

• 50-70-4 D-sorbitol 
• 100-52-7 benzaldehyde 

Downstream Products

• 30608-02-7 2,4-O-benzylidene-L-xylose 
• 141317-08-0 2,4-O-Benzylidene-L-xylose 
• 93164-50-2 2,4-O-benzylidene-5,6-O-isopropylidene-D-glucitol 
• 141393-65-9 2,4-O-Benzylidene-L-xylose-4-nitrophenylhydrazone 
• 141240-04-2 (2S,4S,5R,6S)-4-(Ethoxy-hydroxy-methyl)-6-hydroxymethyl-2-phenyl-[1,3]dioxan-5-ol 
• 794591-52-9 1-O-benzoyl-2,4-O-benzylidene-5,6-O-isopropylidene-3-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-D-glucitol 
• 794591-54-1 2,4-O-benzylidene-5,6-O-isopropylidene-3-O-(β-D-glucopyranosyl)-D-glucitol 
• 794591-49-4 1-O-benzoyl-2,4-O-benzylidene-5,6-O-isopropylidene-D-glucitol 
• 887258-78-8 2,3,5-tri-O-p-methoxybenzyl-1,4-dideoxy-1,4-[[(2R,3S,4R,5R)-2,4-benzylidenedioxy-5,6-isopropylidenedioxy-3-(sulfooxy)hexyl]iminoniumlidene]-L-arabinitol inner salt 
• 887258-77-7 2,3,5-tri-O-p-methoxybenzyl-1,4-dideoxy-1,4-[[(2R,3S,4R,5R)-2,4-benzylidenedioxy-5,6-isopropylidenedioxy-3-(sulfooxy)hexyl]iminoniumlidene]-D-arabinitol inner salt 
• 887258-66-4 2,4-O-benzylidene-5,6-O-isopropylidene-D-glucitol-1,3-cyclic sulfate 

Relevant academic research and scientific papers

A new class of glucosidase inhibitor: Analogues of the naturally occurring glucosidase inhibitor salacinol with different ring heteroatom substituents and acyclic chain extension

Six chain-extended analogues of the naturally occurring glycosidase inhibitor salacinol, with ring-heteroatom variation, were synthesized for structure-activity studies with different glycosidase enzymes. The syntheses involved the reaction of PMB-protect

Synthesis of 2',3'-dideoxy-3'-fluoro-L-ribonucleosides as potential antiviral agents from D-sorbitol

2',3'-Dideoxy-3'-fluoro-L-ribonucleosides were synthesized as potential antiviral agents. The key intermediate, methyl 5-O-benzoyl-2-3-dideoxy-3-fluoro-L-ribofuranoside, which was prepared from D-sorbitol, was condensed with pyrimidine and purine bases to obtain the respective nucleosides. Among them, the cytosine analogue 2',3'-dideoxy-3'-fluoro-α-L-cytidine showed a moderate anti-HBV activity. (C) 2000 Elsevier Science Ltd.