Literature DB >> 21604313

From polyesters to polyamides via O-N acyl migration: an original multi-transfer reaction.

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.
Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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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


  1 in total

1.  Synthesis and mechanistic investigations of pH-responsive cationic poly(aminoester)s.

Authors:  Timothy R Blake; Wilson C Ho; Christopher R Turlington; Xiaoyu Zang; Melanie A Huttner; Paul A Wender; Robert M Waymouth
Journal:  Chem Sci       Date:  2020-02-20       Impact factor: 9.969

  1 in total

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