1606127-89-2

Upstream product

• 100-39-0 benzyl bromide 
• 158226-41-6 6-O-tert-butyldiphenylsilyl-3-deoxy-1,2-O-isopropylidene-α-D-ribo-hexofuranose 
• 1606127-88-1 5-O-benzyl-3,6-dideoxy-6-iodo-1,2-O-isopropylidene-α-D-glucofuranose 
• 1606127-87-0 5-O-benzyl-3-deoxy-1,2-O-isopropylidene-6-O-p-toluenesulphonyl-α-D-glucofuranose 
• 1606127-86-9 5-O-benzyl-3-deoxy-1,2-O-isopropylidene-α-D-glucofuranose 
• 1606127-85-8 C₃₂H₄₀O₅Si 

Downstream Products

• 1606127-75-6 5-O-benzyl-3,6-dideoxy-6-nitro-D-glucono-1,4-lactone 
• 1606127-90-5 5-O-benzyl-3,6-dideoxy-6-nitro-2-O-trifluoromethanesulphonyl-D-glucono-1,4-lactone 
• 1606127-76-7 methyl-5-O-benzyl-3,6-deoxy-6-nitro-β-D-glucofuranoside 
• 1606127-77-8 methyl-5-O-benzyl-3,6-deoxy-6-nitro-α-D-glucofuranoside 

Relevant academic research and scientific papers

Stereocontrolled transformation of nitrohexofuranoses into cyclopentylamines via 2-oxabicyclo[2.2.1]heptanes. Part 6: Synthesis and incorporation into peptides of the first reported 2,3- dihydroxycyclopentanecarboxylic acid

Herein we report the intramolecular alkylation of nitronates of methyl-5-O-benzyl-3,6-deoxy-6-nitro-β-d-glucofuranoside and methyl-5-O-benzyl-3,6-deoxy-6-nitro-α-d-glucofuranoside into the corresponding 2-oxabicyclo[2.2.1]heptane derivatives. Similarly, m