1382059-96-2

Upstream product

• 164665-83-2 2,3-O-isopropylidene-1-O-p-methoxybenzyl-α-D-mannofuranoside 
• 201678-24-2 4-methoxybenzyl 5,6-anhydro-2,3-O-isopropylidene-α-D-mannofuranoside 

Downstream Products

• 1382059-99-5 4-methoxybenzyl 6-deoxy-2,3-O-isopropylidene-5-O-methyl-6-(1H-tetrazol-5-yl)-α-D-mannofuranoside 
• 1382060-00-5 4-methoxybenzyl 5-O-benzyl-6-deoxy-2,3-O-isopropylidene-6-(1H-tetrazol-5-yl)-α-D-mannofuranoside 
• 1382060-22-1 (5S,6S,7R,8S)-7-O-formyl-8-O-methyl-6,7,8,9-tetrahydro-5H-tetrazolo[1,5-a]azepine-5,6,7,8-tetrol 
• 1382060-23-2 (5S,6S,7R,8S)-8-O-benzyl-7-O-formyl-6,7,8,9-tetrahydro-5H-tetrazolo[1,5-a]azepine-5,6,7,8-tetrol 
• 1382059-98-4 4-methoxybenzyl 5-O-benzyl-6-cyano-6-deoxy-2,3-O-isopropylidene-α-D-mannofuranoside 
• 1382059-97-3 4-methoxybenzyl 6-cyano-6-deoxy-2,3-O-isopropylidene-5-O-methyl-α-D-mannofuranoside 

Relevant academic research and scientific papers

Synthesis of tetrazole-fused glycosides by a tandem fragmentation- cyclization reaction

The fragmentation of anomeric alkoxyl radicals (ARF) and the subsequent intramolecular cyclization promoted by hypervalent iodine reagents provide an excellent method for the synthesis of tetrazolo-sugars. This new reaction offers additional advantages for the synthesis of these compounds, including the ready availability of the starting materials, experimental simplicity, mild conditions, and good yields.