936947-80-7

Upstream product

• 13964-23-3 3-azido-3-deoxy-1,2:5,6-di-O-propan-2-ylidene-α-D-allofuranose 
• 14260-27-6 3-deoxy-3-iodo-1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 350255-13-9 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 

Downstream Products

• 936947-81-8 ethyl-3,6-dideoxy-3-benzyloxycarbonylamino-1,2-O-isopropylidene-α-D-xylohept-5-ulofuranuronate 
• 1415917-81-5 C₂₀H₂₄N₄O₇ 
• 1415917-82-6 C₃₃H₄₂N₈O₁₁ 
• 1415917-91-7 C₃₂H₄₀N₈O₁₁ 
• 1415917-92-8 C₃₈H₃₉F₅N₈O₁₁ 
• 1415917-79-1 C₂₁H₂₆N₄O₇ 
• 1334369-92-4 C₁₇H₁₉NO₅ 
• 936947-85-2 2,5-dideoxy-2,5-imino-1,3-di-O-benzyl-1-glycero-α-D-galactoheptitol 
• 936947-84-1 3,6-dideoxy-3,6-(N-benzylamino)-5,7-di-O-benzyl-1,2-O-isopropylidene-α-D-glycero-d-glucohepto-1,4-furanose 
• 936947-82-9 ethyl-3,6-dideoxy-6-diazo-3-benzyloxycarbonylamino-1,2-O-isopropylidene-α-D-xylohept-5-ulofuranuronate 
• 936947-83-0 ethyl-3,6-dideoxy-3,6-benzyloxycarbonylamino-1,2-O-isopropylidene-α-D-xylohept-5-ulofuranuronate 

Relevant academic research and scientific papers

Design and synthesis of regioisomeric triazole based peptidomimetic macrocycles and their dipole moment controlled self-assembly

Two peptidomimetic macrocycles, regioisomeric in terms of the position of triazole/amide, have been synthesized. Both undergo self-assembly in a parallel manner but in solvents of opposite polarity, ascribed to (β, β) and (β-D, β-L) hydrogen bonding leading to formation of two different unique classes of organic nanostructures. The Royal Society of Chemistry.

Rh(II)-catalyzed intramolecular N-H insertion of D-glucose-derived δ-amino α-diazo β-ketoester: Synthesis of pyrrolidine iminosugars

The rhodium acetate catalyzed reaction of D-glucose-derived δ-amino α-diazo β-ketoester allows a stereoselective β-facial intramolecular N-H insertion reaction that leads to formation of the bicyclic pyrrolidinone ring skeleton in high yield. The sugar-su