1415917-91-7

Upstream product

• 1415917-80-4 C₁₃H₂₀N₄O₅ 
• 1415917-79-1 C₂₁H₂₆N₄O₇ 
• 936947-80-7 (5-formyl-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl)-carbamic acid benzyl ester 
• 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 
• 1334369-92-4 C₁₇H₁₉NO₅ 
• 1415917-82-6 C₃₃H₄₂N₈O₁₁ 
• 1415917-81-5 C₂₀H₂₄N₄O₇ 

Downstream Products

• 1415917-92-8 C₃₈H₃₉F₅N₈O₁₁ 

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.