78283-48-4

Upstream product

• 134275-39-1 3-O-benzyl-1,2-O-isopropylidene-β-D-altrofuranose 
• 75-52-5 nitromethane 
• 110316-24-0 3-O-benzyl-1,2-O-isopropylidene-β-D-arabino-pentodialdo-1,4-furanose 
• 908142-25-6 1-2 O-isopropylidene 3-O-benzyl α(D)gluco-pentoaldofuranose 
• 100-39-0 benzyl bromide 
• 350255-13-9 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 23558-05-6 3-O-benzyl-1,2-O-isopropylidene-1,5-D-xylo-dialdofuranose 

Downstream Products

• 69177-83-9 3-O-benzyl-5,6-dideoxy-1,2-O-isopropylidene-6-nitro-α-D-xylo-hex-5-enofuranose 
• 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 
• 141782-04-9 [(S)-1-((3aS,5S,6S,6aS)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-2-nitro-ethyl]-phosphonic acid dimethyl ester 
• 141782-03-8 [(R)-1-((3aS,5S,6S,6aS)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-2-nitro-ethyl]-phosphonic acid dimethyl ester 
• 83603-29-6 3-O-Benzyl-5,6-didesoxy-5-C-(6-isopropyloxycarbonyl-1,3-benzodioxol-5-yl)-1,2-O-isopropyliden-6-nitro-α-D-glucofuranose 
• 83578-85-2 3-O-Benzyl-5,6-didesoxy-5-C-(6-isopropyloxycarbonyl-1,3-benzodioxol-5-yl)-1,2-O-isopropyliden-6-nitro-β-L-idofuranose 
• 83578-88-5 (1R,2S,3S,4S,4aR,11bR)-2,3,4-Tribenzoyloxy-1,3,4,4a,5,11b-hexahydro-1-hydroxy<1,3>dioxolo<4,5-j>phenanthridin-6(2H)-on 
• 83578-89-6 (2S,3R,4S,4aR)-2,3,4-Tribenzoyloxy-3,4,4a,5-tetrahydro<1,3>dioxolo<4,5-j>phenanthridin-6(2H)-on 
• 83578-86-3 (1R,2S,3S,4S,4aR,11bR)-4-Benzyloxy-1,2,3,4,4a,11b-hexahydro-2,3-dihydroxy-1-nitro-6H<1,3>benzodioxolo<5,6-c><1>benzopyran-6-on 
• 99784-34-6 3-O-benzyl-5,6-dideoxy-1,2-O-isopropylidene-6-C-nitro-α-D-xylo-hexanofuranose 

Relevant academic research and scientific papers

Polymeric nanoassembly of imine functionalized magnetite for loading copper salts to catalyze Henry and A3-coupling reactions

Poly(ethylenimine) was grafted on the magnetite (Fe3O4) nanoparticles, and subsequently reacted with different aldehydes to form the imine functionalities (Fe3O4-Imine NPs). Thus formed Fe3O4/su

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.

Orientation of the Addition of Dimethyl Phosphonate to 5,6-Dideoxy-6-nitro-D-hex-5-enofuranoses

The addition of dimethyl phosphonate to six 5,6-dideoxy-6-nitro-D-hex-5-enofuranoses at 25 deg C in the presence of triethylamine preponderantly gave (5R)-adducts, whereas the same reaction at 100 deg C without a base yielded (5S)-adducts as the main products.

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