114181-97-4

Upstream product

• 23558-05-6 3-O-benzyl-1,2-O-isopropylidene-1,5-D-xylo-dialdofuranose 
• 908142-25-6 1-2 O-isopropylidene 3-O-benzyl α(D)gluco-pentoaldofuranose 
• 41545-33-9 3-O-benzyl-6-deoxy-1,2-O-isopropylidene-6-C-nitro-α-L-idofuranose 
• 100-39-0 benzyl bromide 
• 350255-13-9 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 

Downstream Products

• 130222-70-7 3-O-benzyl-5,6-dideoxy-5-C-(dimethoxyphosphinyl)-1,2-O-isopropylidene-α-D-xylo-hexo-5-enofuranose 
• 1197893-88-1 3-((1R)-1-[(5R,6S)-6-benzyloxy-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl]-2-nitroethyl)-2-phenyl-1H-indole 
• 1197893-94-9 3-((1S)-1-[(5R,6S)-6-benzyloxy-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl]-2-nitroethyl)-2-methyl-1H-indole 
• 1197893-86-9 3-((1R)-1-((3aR,5R,6S,6aR)-6-(benzyloxy)-tetrahydro-2,2-dimethylfuro[3,2-d][1,3]dioxol-5-yl)-2-nitroethyl)-2-methyl-1H-indole 
• 99784-35-7 3-O-benzyl-5,6-dideoxy-6-C-nitro-α-D-xylo-hexanofuranose 
• 99784-36-8 (2S,3R)-2-(benzyloxy)-3-(formyloxy)-5-nitropentanal 
• 99784-34-6 3-O-benzyl-5,6-dideoxy-1,2-O-isopropylidene-6-C-nitro-α-D-xylo-hexanofuranose 
• 113713-85-2 [(R)-1-((3aR,5S,6R,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-2-nitro-ethyl]-phosphonic acid dimethyl ester 
• 113713-83-0 [(S)-1-((3aR,5S,6R,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-2-nitro-ethyl]-phosphonic acid dimethyl ester 

Relevant academic research and scientific papers

Solvent and catalyst free route to 3-indolyl glycoconjugates: Synthesis of sugar tethered isoxazolines and isoxazoles from 3-indolyl nitroalkanes

An expedient, solvent and catalyst free strategy for the synthesis of sugar based bis(indolyl)methanes and indolyl nitroalkanes has been developed. The protocol works well within a wide range of substrates, and tolerates various N/O protecting groups. The

Glycosynthase-Mediated Assembly of Xylanase Substrates and Inhibitors

An exo-β-xylosidase mutant with glycosynthase activity was created to aid in the synthesis of xylanase substrates and inhibitors. Simple monosaccharides were easily elaborated into di-, tri- and tetrasaccharides by using this enzyme. Some products proved