106761-49-3

Upstream product

• 57099-04-4 3-O-benzyl-1,2-O-isopropylidene-α-D-allofuranose 
• 76-83-5 trityl chloride 
• 106734-68-3 3-O-benzyl-1,2-isopropylidene-6-O-triphenylmethyl-α-D-allo-hexofuran-5-ulose 
• 100-39-0 benzyl bromide 
• 22331-21-1 1,2:5,6-di-O-isopropylidene-3-O-benzyl-α-D-allofuranose 
• 14686-89-6 (1,2:5,6)-di-O-isopropylidene-D-gulose 

Downstream Products

• 1126643-53-5 3-O-benzyl-5,6-dideoxy-1,2-O-isopropylidene-α-D-ribo-5-enoheptofuranurono-7,5'-lactone 

Relevant academic research and scientific papers

Synthesis of pseudo-C-nucleosides from β-formyl-α,β- unsaturated ester bearing a β-furanosidic moiety

Pseudo-C-nucleosides have potential biological activity, and an efficient synthesis of new pseudo-C-nucleosides has been developed via the reaction of a β-formyl-α,β-unsaturated ester bearing a β-sugar moiety with hydrazines in neutral and acidic conditio

SYNTHESIS OF TWO RIGID DIACYLGLYCEROL ANALOGUES HAVING A PERHYDRO FUROFURAN BIS-γ-BUTYROLACTONE SKELETON. 3.

The stereoselective synthesis of two new bis-γ-butyrolactones starting from 1,2:5,6-di-O-isopropylidene-α-D-allofuranose was completed in 22 steps.One of the isomers (3a) showed very good binding affinity towards protein kinase C.