553681-62-2

Upstream product

• 136738-59-5 2,6-anhydro-5,7-O-benzylidene-1-deoxy-1-nitro-D-glycero-D-gulo-heptitol 
• 849834-82-8 C-(4,6-O-benzylidene-β-D-glucopyranosylomethyl) hydroxylamine 
• 849834-83-9 C-(4,6-O-benzylidene-β-D-glucopyranosyl) formaldoxime 
• 849834-84-0 (2R,4aR,6R,7R,8R,8aS)-6-((2R,4aR,7S,8aR,9R,9aS,10aS)-9-Hydroxy-2-phenyl-octahydro-1,3,8,10-tetraoxa-6-aza-anthracen-7-yl)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine-7,8-diol 

Relevant academic research and scientific papers

Synthesis of glycosyl amino acids by light-induced coupling of photoreactive amino acids with glycosylamines and 1-C-aminomethyl glycosides

The glycosylamines of O-acetyl-protected GlcNAc and chitobiose, as well as two partially unprotected 1-C-aminomethyl glucosides, were photochemically coupled with orthogonally protected N-aspartyl-5-bromo-7-nitroindoline derivatives. The reactions proceed

Selective reductions of C-(4,6-O-benzylidene-β-D-glucopyranosyl) nitromethane

The nitromethyl group of C-(4,6-O-benzylidene-β-D-glucopyranosyl) nitromethane was manipulated by various reduction and oxidation methods and further functionalizations into -CH2NHOH, -CH=NOH, -CN, -CH=O, and -CH2- NHCONH2