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Cited by 589

The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.

Peptidomimetics via copper-catalyzed azide–alkyne cycloadditions

Angell, Yu L., Burgess, Kevin·2007·Chemical Society Reviews

Abstract

This critical review concerns the impact of copper-mediated alkyne-azide cycloadditions on peptidomimetic studies. It discusses how this reaction has been used to insert triazoles into peptide chains, to link peptides to other functionalities (e.g. carbohydrates, polymers, and labels), and as a basis for evolution of less peptidic compounds as pharmaceutical leads. It will be of interest to those studying this click reaction, peptidomimetic secondary structure and function, and to medicinal chemists.

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Crossref · 10.1039/b701444a

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Metadata

Authors
Angell, Y. L., & Burgess, K.
Venue
Chemical Society Reviews
Published
2007
Volume
36
Issue
10
Pages
1674
ISSN
  • 0306-0012 (ISSN-L)
  • 1460-4744
OpenAlex
W2015235532
Cited by
589
References
3
FWCI
1.54
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Peptidomimetics via copper-catalyzed azide–alkyne cycloadditions. https://app.cochat.ai/papers/10.1039/b701444a
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Angell, Y. L., & Burgess, K. (2007). Peptidomimetics via copper-catalyzed azide–alkyne cycloadditions. Chemical Society Reviews. https://doi.org/10.1039/b701444a

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.