1437656-93-3

Upstream product

• 1437656-83-1 2,3,5-tri-O-benzyl-4-deoxy-4-azido-D-xylose 
• 1437657-83-4 2,3,5-tri-O-benzyl-4-deoxy-4-azido-D-xylitol 
• 1437657-80-1 2,3,5-tri-O-benzyl-4-deoxy-4-azido-1-O-trityl-D-xylitol 
• 1437657-77-6 2,3,5-tri-O-benzyl-4-O-methanesulfonyl-1-O-trityl-L-arabinitol 
• 1437657-74-3 2,3,5-tri-O-benzyl-1-O-trityl-L-arabinitol 
• 96192-07-3 2,3,5-tri-O-benzyl-L-arabinofuranose 

Downstream Products

• 1437657-16-3 C₃₈H₄₆N₂O₅ 
• 1437657-19-6 C₃₈H₄₆N₂O₅ 
• 1437657-10-7 C₃₆H₄₄N₂O₅ 
• 1437657-13-0 C₃₆H₄₄N₂O₅ 
• 1437657-52-7 C₃₃H₄₀N₂O₄ 
• 1437657-46-9 C₃₁H₃₈N₂O₄ 

Relevant academic research and scientific papers

Chiral pyrroline-based Ugi-three-component reactions are under kinetic control

Although it is often assumed that the stereochemistry in Ugi multicomponent reactions is determined in the final Mumm rearrangement step, experimental and computational evidence that Ugi reactions on hydroxylated pyrrolines proceed under kinetic control is reported. The stereochemistry of the reaction is established with the addition of the isocyanide to the intermediate iminium ion, whose conformation is determined by its substitution pattern.