Click and Multicomponent Reactions Work Together for Polymer Chemistry

Umit Tunca*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

51 Citations (Scopus)

Abstract

This article investigates the current combinations of click and multicomponent reactions (MCRs) to produce complex macromolecular structures through polymer–polymer conjugation or hetero-functionalization of polymers. The click and MCRs display similar features covering the equimolarity, fast time scale, high yields, stable compounds, modular, orthogonal and single reaction trajectory. Of classical click reactions, CuAAC, Diels–Alder, thiol-ene (-yne), and nucleophilic substitution on perfluoroaryl groups reactions are combined with MCRs, namely, Passerini, Ugi, or Biginelli reactions. It should be noted that these combinations can afford the target polymer structures, which are not attainable by employing one of these reactions alone.

Original languageEnglish
Article number1800163
JournalMacromolecular Chemistry and Physics
Volume219
Issue number16
DOIs
Publication statusPublished - Aug 2018

Bibliographical note

Publisher Copyright:
© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim

Keywords

  • Biginelli reactions
  • click reactions
  • copper-catalyzed azide–alkyne cycloaddition reactions
  • Diels–Alder reactions
  • multicomponent reactions
  • Passerini reactions
  • thiol-ene reactions
  • Ugi reactions

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