Abstract
The cationic ring-opening polymerization of 1-azabicyclo[4.2.0]octane, commonly called conidine (1) was studied with some chiral tricyclic amino acid esters (6a–6f) as acylation agents to obtain optically active biopolymers (8a–8f) of the different masses. The structures of the new compounds were confirmed by FT-IR, UV and NMR, and the distribution index of the molecular weights of the polymers was determined from SEC measurements.
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