POLYMERIZATION OF 1-AZABICYCLO[4.2.0]OCTANE WITH CHIRAL TRICYCLIC AMINO ACID ESTERS FOR OBTAINING BIOMEDICAL MATERIALS

Cigdem Yolacan; Irem Kulu; Nuket Ocal

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POLYMERIZATION OF 1-AZABICYCLO[4.2.0]OCTANE WITH CHIRAL TRICYCLIC AMINO ACID ESTERS FOR OBTAINING BIOMEDICAL MATERIALS

Papers | Updated：2021-06-21

- POLYMERIZATION OF 1-AZABICYCLO[4.2.0]OCTANE WITH CHIRAL TRICYCLIC AMINO ACID ESTERS FOR OBTAINING BIOMEDICAL MATERIALS
- Vol. 28, Issue 1, Pages: 39-44(2010)
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- Published：20 January 2010
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Cigdem Yolacan, Irem Kulu, Nuket Ocal. POLYMERIZATION OF 1-AZABICYCLO[4.2.0]OCTANE WITH CHIRAL TRICYCLIC AMINO ACID ESTERS FOR OBTAINING BIOMEDICAL MATERIALS[J]. 2010, 28(1): 39-44.
DOI：

Cigdem Yolacan, Irem Kulu, Nuket Ocal. POLYMERIZATION OF 1-AZABICYCLO[4.2.0]OCTANE WITH CHIRAL TRICYCLIC AMINO ACID ESTERS FOR OBTAINING BIOMEDICAL MATERIALS[J]. 2010, 28(1): 39-44. DOI：

摘要

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.

Abstract

The cationic ring-opening polymerization of 1-azabicyclo[4.2.0]octane

UV and NMR

and the distribution index of the molecular weights of the polymers was determined from SEC measurements.

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