146986-45-0

Upstream product

• 100-39-0 benzyl bromide 
• 250662-84-1 (3aR,5S,6S,6aR)-2,2-dimethyl-6-(prop-2-ynyloxy)tetrahydrofuro[2,3-d][1,3]dioxole-5-carbaldehyde 
• 108-24-7 acetic anhydride 
• 41341-99-5 3,5-di-O-benzyl-1,2-O-isopropylidene-α-D-xylofuranose 
• 100-44-7 benzyl chloride 
• 20031-21-4 1,2-O-isopropylidene-α-D-xylose 
• 16054-77-6 3,5-di-O-benzyl-D-xylofuranose 

Downstream Products

• 1439518-89-4 C₂₈H₂₆O₄S 
• 1439518-97-4 C₂₈H₂₆O₄S 
• 1439516-88-7 C₂₈H₂₉BrO₄S 
• 1439517-11-9 C₂₈H₂₉BrO₄S 
• 1439519-69-3 C₂₈H₂₈O₄S 
• 1439519-77-3 C₂₈H₂₈O₄S 
• 1439516-80-9 C₂₈H₂₇BrO₄S 
• 1439517-03-9 C₂₈H₂₇BrO₄S 
• 1439516-72-9 C₂₇H₂₇BrO₅S 
• 1439516-96-7 C₂₇H₂₇BrO₅S 
• 1613288-47-3 2-acetamido-6-chloro-9-(2-O-acetyl-3,5-di-O-benzyl-β-D-xylofuranosyl)purine 
• 1613288-48-4 2-acetamido-6-chloro-9-(2-O-acetyl-3,5-di-O-benzyl-β-D-xylofuranosyl)purine 

Relevant academic research and scientific papers

Design and synthesis of carbohydrate based medium sized sulfur containing benzannulated macrocycles: Applications of Sonogashira and Heck coupling

Palladium catalyzed intramolecular Sonogashira and Heck coupling reactions have been applied for diversity-oriented synthesis of sulfur containing carbohydrate based medium sized ring macrocycles. The process involves design and synthesis of building bloc

Syntheses and conformational studies on AZT and its deuterated analogues

The NMR spectrum of 3′-azido-3′-deoxythymidine (AZT) in aqueous solution provides sum of some of the proton-proton coupling constants. This limitation precludes the determination of the pseudorotational parameters of the sugar ring. Selective deuteration alleviates this problem. The synthesis of 2′-deutero and 3′-deutero- AZT have been described for the first time starting from D-xylose and β-thymidine respectively. NMR study of these analogues in aqueous solutions shows that almost equal amount of C-2′-endo and C-3′-endo species exist in equilibrium.