53931-26-3

Upstream product

• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 558-13-4 carbon tetrabromide 
• 23558-05-6 3-O-benzyl-1,2-O-isopropylidene-1,5-D-xylo-dialdofuranose 
• 18685-18-2 3-O-benzyl-1,2-5,6-O-diisopropylidene-α-D-glucofuranose 
• 100-39-0 benzyl bromide 
• 22529-61-9 (1R)-1-((3aR,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro(2,3-d)(1,3)dioxol-5-yl)ethane-1,2-diol 

Downstream Products

• 117174-46-6 (3aR,5R,6S,6aR)-6-(benzyloxy)-5-ethynyl-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxole 
• 59578-22-2 3-O-benzyl-6-bromo-5,6-didesoxy-1,2-O-isopropylidene-α-D-xylo-hex-5-ynofuranose 
• 66108-68-7 (6-²H)-3-O-benzyl-5,6-dideoxy-1,2-O-isopropylidene-α-D-xylo-hex-5-yno-furanose 
• 66108-69-8 C₂₀H₂₅⁽²⁾HO₄ 
• 78942-98-0 (3-O-benzyl-5,6-didesoxy-1,2-O-isopropylidene-α-D-xylo-hex-5-ynofuranos-6-yl)phosphonate de diethyle 
• 934493-25-1 6-benzyloxy-2,2-dimethyl-5-(1-methylene-allyl)-tetrahydro-furo[2,3-d][1,3]dioxole 
• 93228-23-0 (6R)-(6-²H₁)-5,6-O-diacetyl-3-O-benzyl-1,2-O-isopropylidene-α-D-glucofuranose 
• 93170-75-3 (6S)-(6-²H₁)-5,6-O-diacetyl-3-O-benzyl-1,2-O-isopropylidene-α-D-glucofuranose 
• 66108-74-5 C₁₆H₂₁⁽²⁾HO₆ 
• 66108-75-6 (6R)-(6-²H₁)-3-O-benzyl-1,2-O-isopropylidene-α-D-glucofuranose 
• 66108-73-4 (6S)-(6-²H₁)-3-O-benzyl-1,2-O-isopropylidene-α-D-glucofuranose 
• 66108-72-3 (E)-(6-²H₁)-3-O-benzyl-5,6-dideoxy-1,2-O-isopropylidene-α-D-xylo-hex-5-enofuranose 
• 93170-77-5 (Z)-(6-²H₁)-3-O-benzyl-5,6-dideoxy-1,2-isopropylidene-α-D-xylo-hex-5-enofuranose 
• 93170-78-6 C₁₆H₂₁⁽²⁾HO₄ 

Relevant academic research and scientific papers

A new versatile strategy for C-aryl glycosides

(Chemical Equation Presented) A versatile strategy involving a sequential intermolecular enyne metathesis of C-alkynyl glycosides with ethylene, Diels-Alder, and aromatization reactions is successfully developed to provide a range of C-aryl glycosides.

SYNTHESIS OF D-(6R)- AND D-(6S)-(6-2H1)GLUCOSE

Chemical synthesis of D-(6R)- and D-(6S)-(6-2H1)glucose is described comprising (i) formation of (6-2H1)-3-O-benzyl-5,6-dideoxy-1,2-O-isopropylidene-α-D-xylo-hex-5-ynofuranose from D-glucose; (ii) stereospecific

Preparation de derives de sucres acetyleniques terminaux et d'acides ynuroniques par reaction de Wittig

The method described for the preparation of terminal acetylenic sugars presents two advantages over earlier procedures: no new asymmetric center is created and the chain can be extended by one or more C-atoms.The method also allows preparation of ynuronic