| Literature DB >> 21604313 |
Julien Tailhades1, Sébastien Blanquer, Benjamin Nottelet, Jean Coudane, Gilles Subra, Pascal Verdié, Etienne Schacht, Jean Martinez, Muriel Amblard.
Abstract
A new strategy for the synthesis of polyamides from polyesters of hydroxyl-containing amino acids using a multi O-N acyl transfer reaction was developed. This original approach allowed the synthesis of three generations of polymers from the same starting monomer. The polymerization of N-benzyloxycarbonyl-serine and its γ-homologated derivative provided the Z-protected polyesters; then the water-soluble polycationic polyesters were obtained by removal of the Z-protecting group; and finally the polyamides were obtained by a base-induced multi O-N acyl transfer, both in aqueous or organic medium. The key step transfer reaction was monitored by the disappearance and appearance of characteristic NMR proton signals and IR bands of polyesters and polyamides.Entities:
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Year: 2011 PMID: 21604313 DOI: 10.1002/marc.201100235
Source DB: PubMed Journal: Macromol Rapid Commun ISSN: 1022-1336 Impact factor: 5.734