Preparation of biohybrid amphiphiles via the copper catalysed Huisgen [3 + 2] dipolar cycloaddition reaction
- 2 August 2005
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- No. 33,p. 4172-4174
- https://doi.org/10.1039/b508428h
Abstract
Biohybrid amphiphiles have been prepared from terminal azide functionalised polystyrene and an alkyne functionalised peptide or protein via a Cu(I) catalysed Huisgen [3 + 2] dipolar cycloaddition reaction.Keywords
This publication has 25 references indexed in Scilit:
- Step-Growth “Click” Coupling of Telechelic Polymers Prepared by Atom Transfer Radical PolymerizationMacromolecules, 2005
- Cysteine-Reactive Polymers Synthesized by Atom Transfer Radical Polymerization for Conjugation to ProteinsJournal of the American Chemical Society, 2004
- Site-specific PEGylation of proteins containing unnatural amino acidsBioorganic & Medicinal Chemistry Letters, 2004
- Click chemistry in materials synthesis. 1. Adhesive polymers from copper‐catalyzed azide‐alkyne cycloadditionJournal of Polymer Science Part A: Polymer Chemistry, 2004
- Solid-Phase ATRP Synthesis of Peptide−Polymer HybridsJournal of the American Chemical Society, 2004
- Bioconjugation by Copper(I)-Catalyzed Azide-Alkyne [3 + 2] CycloadditionJournal of the American Chemical Society, 2003
- Giant Amphiphiles by Cofactor ReconstitutionAngewandte Chemie International Edition in English, 2002
- A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal AlkynesAngewandte Chemie International Edition in English, 2002
- The Formation of Polymer Vesicles or “Peptosomes” by Polybutadiene-block-poly(l-glutamate)s in Dilute Aqueous SolutionJournal of the American Chemical Society, 2002
- Synthesis of well‐defined azido and amino end‐functionalized polystyrene by atom transfer radical polymerizationMacromolecular Rapid Communications, 1997