Bringing Efficiency to Materials Synthesis: The Philosophy of Click Chemistry
- 1 January 2007
- journal article
- editorial
- Published by CSIRO Publishing in Australian Journal of Chemistry
- Vol. 60 (6) , 381-383
- https://doi.org/10.1071/ch07107
Abstract
Australian Journal of Chemistry - an International Journal for Chemical Science publishes research papers from all fields of chemical science.Keywords
This publication has 16 references indexed in Scilit:
- 1,3‐Dipolar Cycloadditions of Azides and Alkynes: A Universal Ligation Tool in Polymer and Materials ScienceAngewandte Chemie International Edition in English, 2007
- Versatile Pathway to Functional Telechelics via RAFT Polymerization and Click ChemistryMacromolecules, 2007
- The Rise of Azide–Alkyne 1,3-Dipolar 'Click' Cycloaddition and its Application to Polymer Science and Surface ModificationAustralian Journal of Chemistry, 2007
- Structurally Diverse Dendritic Libraries: A Highly Efficient Functionalization Approach Using Click ChemistryMacromolecules, 2005
- Biological–synthetic hybrid block copolymers: Combining the best from two worldsJournal of Polymer Science Part A: Polymer Chemistry, 2004
- Click chemistry in materials synthesis. 1. Adhesive polymers from copper‐catalyzed azide‐alkyne cycloadditionJournal of Polymer Science Part A: Polymer Chemistry, 2004
- Efficiency and Fidelity in a Click‐Chemistry Route to Triazole Dendrimers by the Copper(I)‐Catalyzed Ligation of Azides and AlkynesAngewandte Chemie International Edition in English, 2004
- Bioconjugation by Copper(I)-Catalyzed Azide-Alkyne [3 + 2] CycloadditionJournal of the American Chemical Society, 2003
- Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to AzidesThe Journal of Organic Chemistry, 2002
- Click Chemistry: Diverse Chemical Function from a Few Good ReactionsAngewandte Chemie International Edition in English, 2001