547769-48-2

Upstream product

• 91882-92-7 3-O-allyl-1,2-O-isopropylidene-α-D-glucofuranose 
• 50-99-7 D-glucose 
• 547769-42-6 (3S,4R,3a'R,5'R,6'S,6a'R)-4-(6'-allyloxy-2',2'-dimethyl-tetrahydrofuro[2',3'-d][1',3']dioxol-5'-yl)-1-(4-methoxyphenyl)-3-phenoxy-azetidin-2-one 
• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 152185-56-3 3-O-Allyl-1,2-O-isopropylidene-α-D-xylo-pentodialdose 
• 20316-77-2 (3aR,5R,6S,6aR)-6-(allyloxy)-5-((R)-2,2-dimethyl[1,3]dioxolan-4-yl)-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxole 

Relevant academic research and scientific papers

Asymmetric synthesis of azetidin-2-ones by [2+2] cycloaddition using chiral imines derived from D-(+)-glucose

Asymmetric synthesis of β-lactams by the [2+2] cycloaddition of ketenes with chiral imines derived from D-(+)-glucose was carried out; predominantly cis-β-lactams were formed with very high diastereoselectivity. The stereochemistry at C-3 and C-4 was esta