Copper‐Catalyzed Azide–Alkyne Click Chemistry for Bioconjugation

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Copper-Catalyzed Azide-Alkyne Click Chemistry for Bioconjugation.

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Copper(I)-catalyzed 1,3-dipolar cycloaddition of azides and terminal alkynes (CuAAC), better known as "click" reaction, has triggered the use of 1,2,3-triazoles in bioconjugation, drug discovery, materials science and combinatorial chemistry. Here we report a new series of water-soluble catalysts based on N-heterocyclic carbene (NHC)-Cu complexes which are additionally functionalized with a sul...

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Thiol–ene click chemistry: a biocompatible way for orthogonal bioconjugation of colloidal nanoparticles† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c7sc01447c Click here for additional data file.

Molecular Science and Biomedicine L Chemo/Bio-Sensing and Chemometrics, Chemistry and Chemical Engineering, A Province, Hunan University, Changsha, Hun ac.cn. Center for Research at Bio/Nano Interface, Physiology and Functional Genomics, Heal McKnight Brain Institute, University of Fl USA. E-mail: [email protected].edu George & Josephine Butler Polymer Researc Science & Engineering, Department of Che...

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ژورنال

عنوان ژورنال: Current Protocols in Chemical Biology

سال: 2011

ISSN: 2160-4762,2160-4762

DOI: 10.1002/9780470559277.ch110148