443299-13-6

Upstream product

• 443299-12-5 bis-(3-azido-benzyl)-[1-(3-azido-phenyl)-ethyl]-amine 
• 22031-12-5 [2-((diphenylphospino)methyl)-2-methyl-1,3-propanediyl]bis[diphenylphosphine] 
• 443299-17-0 1-(3-azidophenyl)ethylamine 
• 443299-18-1 3-azidobenzyl iodide 

Relevant academic research and scientific papers

Helical sense bias induced by point chirality in cage compounds

Highly efficient chirality transfer is employed in controlling the topological asymmetry of chiral cages with propeller-like shape and pseudo C3 symmetry (see picture; R=H, Cl). The cages are formed when two tripodal units (a tribenzylamine and