729596-15-0

Upstream product

• 108788-49-4 ethyl (E)-[3-O-benzyl-5,6-dideoxy-1,2-O-isopropylidene-α-D-gluco]-heptofuran-5-en-uronate 

Downstream Products

• 729596-25-2 3,5,7-tri-O-acetyl-6-(N-benzyloxycarbonylamino)-6-deoxy-1,2-O-isopropylidene-α-D-glycero-D-gluco-heptofuranose 
• 729596-19-4 6-benzyloxycarbonylamino-6-deoxy-1,2-O-isopropylidene-α-D-glycero-D-gluco-hepto-1,4-furanose 
• 729596-18-3 ethyl 6-azido-6-deoxy-3-O-benzyl-1,2-O-isopropylidene-α-D-glycero-D-gluco-heptofuranuronate 

Relevant academic research and scientific papers

Asymmetric dihydroxylation of D-glucose derived α,β-unsaturated ester: Synthesis of azepane and nojirimycin analogues

The asymmetric dihydroxylation of a D-glucose derived α,β- unsaturated ester 3 afforded syn vicinal diols in good to high diastereoselectivity. The conversion of these vicinal diols to the corresponding cyclic sulfate, regio-, stereoselective nucleophilic