86495-59-2

Upstream product

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

Downstream Products

• 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 
• 103526-89-2 3-O-Benzyl-5-deoxy-1,2-O-isopropylidene-5-C-methylene-β-L-arabino-hexofuranurononitrile 
• 103526-87-0 5,6-Dideoxy-1,2-O-isopropylidene-3-O-benzyl-5-C-methylene-α-D-xylo-hexofuranurononitrile 
• 152434-63-4 C₂₄H₂₅NO₉ 
• 181049-36-5 (S)-2-((3aR,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-3-nitro-propionaldehyde 
• 181049-42-3 3-O-benzyl-5-deoxy-1,2-O-isopropylidene-5-nitromethyl-α-D-glucofuranose 
• 847984-53-6 3-O-benzyl-5,6-dideoxy-5-C-(1',4'-dimethoxynaphthalen-2'-yl)-1,2-O-isopropylidene-6-nitro-β-L-idofuranose 
• 1356060-39-3 3-O-benzyl-5,6-dideoxy-5-C-(3'-hydroxy-1',4'-naphthoquinon-2'-yl)-1,2-O-isopropylidene-6-nitro-α-D-glucofuranose 
• 1356060-41-7 (6bR,7R,8S,9S,10S,10aR)-8-(benzyloxy)-7,9,10-trihydroxy-6b,7,8,9,10,10a-hexahydro-11H-benzo[a]carbazole-5,6-dione 
• 1356060-40-6 2-((1R,2R,3S,4S,5S,6R)-3-(benzyloxy)-2,4,5-trihydroxy-6-nitrocyclohexyl)-3-hydroxynaphthalene-1,4-dione 
• 847984-56-9 (1R,2S,3S,4R,5S,6S)-3-(benzyloxy)-5-(1,4-dimethoxynaphthalen-2-yl)-1,2,4-trihydroxy-6-nitrocyclohexane 
• 847984-57-0 (1R,2S,3S,4R,5S,6S)-6-amino-3-(benzyloxy)-5-(1',4'-dimethoxynaphthalen-2'-yl)cyclohexane-1,2,4-triol 

Relevant academic research and scientific papers

CHIRALE SYNTHESE VON (+)-LYCORICIDIN

The synthesis of (+)-lycoricidine from D-glucose is described.Addition of the carbanion 11 to the nitroolefine 10 yields the adduct 12+13, from which crystalline lactone 16 with muco-configuration in the cyclitol-ring can be isolated after hydrolysis and

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

Synthesis of densely functionalised C-glycosides by a tandem oxy Michael addition-Wittig olefination pathway

Wittig olefination of 5,6-dideoxy-5,6-anhydro-6-nitro-d-glucofuranose (5) triggered a concomitant cyclisation via oxy Michael addition of the C2-hydroxyl group resulting in the formation of C-vinyl glycosides with Z-olefinic geometry.