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Cited by 1,029

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Analysis and Optimization of Copper‐Catalyzed Azide–Alkyne Cycloaddition for Bioconjugation

Open access
Hong, Vu, Presolski, Stanislav I., Ma, Celia, Finn, M. G.·2009·Angewandte Chemie International Edition

Abstract

How to click with biomolecules: Copper-catalyzed azide–alkyne cycloaddition has been optimized for use with biological molecules. The key development is the addition of two reagents that allow ascorbate to be used as reducing agent whilst eliminating problems caused by copper ascorbate side reactions. The result is a robust, rapid, and convenient procedure for the modification of proteins, DNA, RNA, and other biomolecules (see scheme).

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Metadata

Authors
Hong, V., Presolski, S. I., Ma, C., & Finn, M. G.
Venue
Angewandte Chemie International Edition
Publisher
Wiley
Published
2009-12-15
Volume
48
Issue
52
Pages
9879-9883
ISSN
  • 1433-7851 (ISSN-L)
  • 1521-3773
OpenAlex
W2165286214
Cited by
1,029
References
1
FWCI
28.10
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Analysis and Optimization of Copper‐Catalyzed Azide–Alkyne Cycloaddition for Bioconjugation. https://app.cochat.ai/papers/10.1002/anie.200905087
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Hong, V., Presolski, S. I., Ma, C., & Finn, M. G. (2009). Analysis and Optimization of Copper‐Catalyzed Azide–Alkyne Cycloaddition for Bioconjugation. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.200905087

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