152501-46-7

Upstream product

• 152501-37-6 ethyl 3,4-di-O-acetyl-2-chloro-2-deoxy-1-thio-α-L-rhamnopyranoside 
• 152501-41-2 ethyl 2-chloro-2-deoxy-1-thio-α-L-rhamnopyranoside 
• 98-88-4 benzoyl chloride 
• 69980-52-5 2,3,4-tri-O-acetyl-L-rhamnopyranosyl bromide 
• 152501-44-5 ethyl 4-O-benzoyl-2-chloro-2-deoxy-1-thio-α-L-rhamnopyranoside 

Relevant academic research and scientific papers

Synthesis of chlorodeoxy trisaccharides related to the Shigella flexneri Y polysaccharide

Chloromethoxylation of di-O-acetyl-L-rhamnal has been employed as a convenient route to methyl 3,4-di-O-acetyl-2-chloro-2-deoxy-α-L-rhamnopyranoside 7, which was converted into an ethyl thioglycoside 10, suitable for use as a glycosyl donor.It and a disaccharide analogue 20 were effective donors in N-iodosuccinimide-triflic acid promoted glycosylations of a 2-acetamido-2-deoxy-D-glucopyranoside acceptor 22.Chlorodeoxy saccharides have previously been shown to be suitable derivatives to probe oligosaccharide-protein interactions, and this synthetic strategy provided three monochlorodeoxy trisaccharide congeners of the native Shigella flexneri epitope 2, α-L-Rha p-(1->3)-α-L-Rha p-(1->3)-β-D-GlcNAc p-(1->O)-Me.