The purpose of this research was to synthesize new regular poly(ester amide)s (PEAs) consisting of nontoxic building blocks like hydrophobic ␣-amino acids, ␣,-diols, and aliphatic dicarboxylic acids, and to examine the effects of the structure of these building block components on some physico-chemi
Amino acid based bioanalogous polymers. Synthesis of novel poly(urethane amide)s based on N,N′-(trimethylenedioxydicarbonyl)bis(phenylalanine)
✍ Scribed by Tamara Kartvelishvili; Akaki Kvintradze; Ramaz Katsarava
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 409 KB
- Volume
- 197
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
The feasibility of synthesizing high-molecular-weight amino acid based bioanalogous polymers (AABBPs)-poly(urethane amide)s (PUA) -via polycondensation (PC) of dip-nitrophenyl ester of N,~-(trimethylenedioxydicarbonyl)bis(L-phenylalanine) (3) with diamines or their derivatives under mild conditions in organic solvents was studied for the first time. A regular PUA (q,,,, = 1,53 dL/g) was obtained by PC of 3 with hexamethylenediamine. A dipeptide (Phe-Phe) containing regular poly(ester urethane amide) (q,,,, = 0,58 dL/g) was synthesized by PC of 3 with p-toluenesulfonic acid salt of bis(L-phenylalanine) 1,4-butylene diester. A tripeptide (Phe-Lys-Phe) containing PUA (qred = 0,38 dL/g) with pendent ester groups was prepared via PC of 3 with N,N-bis(trimethylsily1)-L-lysine methyl ester. These novel AABBPs which may be considered as structural analogs of AB type bioanalogous polymers -conventional poly(amino acids) are of interest in enzymology, immunology, pharmacology, and biotechnology (as materials for biomedical applications).
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