108788-47-2

Upstream product

• 108182-63-4 (E)-3-O-benzyl-5,6-dideoxy-1,2-O-isopropylidene-α-D-xylo-hept-5-eno-1,4-furanose 
• 23558-05-6 3-O-benzyl-1,2-O-isopropylidene-1,5-D-xylo-dialdofuranose 
• 108788-49-4 ethyl (E)-[3-O-benzyl-5,6-dideoxy-1,2-O-isopropylidene-α-D-gluco]-heptofuran-5-en-uronate 
• 195519-71-2 3-O-benzyl-5,6-dideoxy-1,2-dideoxy-1,2-O-isopropylidene-α-D-xylohept-5-eno-1,4-furanose 

Downstream Products

• 1224467-46-2 5-azido-3-O-benzyl-5-deoxy-1,2-O-isopropylidene-α-D-glycero-D-gluco-hepto-1,4-furanose 
• 108788-53-0 6-azido-3-O-benzyl-6-deoxy-1,2-O-isopropylidene-β-L-glycero-L-ido-hepto-1,4-furanose 
• 108788-57-4 6-azide-3-O-benzyl-6-deoxy-1,2-O-isopropylidene-7-O-p-toluenesulfonyl-α-L-glycero-L-ido-heptofuranose 
• 108788-61-0 5,7-anhydro-6-azide-3-O-benzyl-6-deoxy-1,2-O-isopropylidene-α-L-glycero-L-ido-heptofuranose 
• 108788-65-4 5,7-anhydro-6-N-benzyloxycarbonylamino-6-deoxy-1,2-O-isopropylidene-α-L-glycero-L-ido-heptofuranose 
• 108788-69-8 1,3-anhydro-2-N-benzyloxycarbonylamino-2-deoxy-L-glycero-D-gluco-heptitol 

Relevant academic research and scientific papers

Synthesis of azepane and nojirimycin iminosugars: the Sharpless asymmetric epoxidation of d-glucose-derived allyl alcohol and highly regioselective epoxide ring opening using sodium azide

The Sharpless asymmetric epoxidation of d-glucose-derived allyl alcohol 4 afforded α- and β-epoxides 5a and 5b in high stereoselectivity. The epoxide ring opening in 5a/5b was studied with different nucleophilic azido reagents, under various reaction cond