The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Head‐to‐Tail Peptide Cyclodimerization by Copper‐Catalyzed Azide–Alkyne Cycloaddition
Abstract
Rings forged with copper: Oligopeptide cyclodimerization occurs selectively when precursors containing azide and alkyne groups are exposed to copper(I) ions on polystyrene supports (see picture; Prot=protecting group).
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Citations
Cites
Tornøe, C. W., Christensen, C., & Meldal, M. (2002) · The Journal of Organic Chemistry · doi:10.1021/jo011148j · Cited by 8,696
Cited by
CuI‐Catalyzed Alkyne–Azide “Click” Cycloadditions from a Mechanistic and Synthetic Perspective
Bock, V. D., Hiemstra, H., & van Maarseveen, J. H. (2006) · European Journal of Organic Chemistry · doi:10.1002/ejoc.200500483 · Cited by 1,452
Contemporary strategies for peptide macrocyclization
White, C. J., & Yudin, A. K. (2011) · Nature Chemistry · doi:10.1038/nchem.1062 · Cited by 1,088
“Click”‐Chemistry in Polymer and Material Science: the Update
Binder, W. H. (2008) · Macromolecular Rapid Communications · doi:10.1002/marc.200800332 · Cited by 567
Metadata
- Authors
- Punna, S., Kuzelka, J., Wang, Q., & Finn, M. G.
- Venue
- Angewandte Chemie International Edition
- Publisher
- Wiley
- Published
- 2005-04-06
- Volume
- 44
- Issue
- 15
- Pages
- 2215-2220
- ISSN
- 1433-7851 (ISSN-L)
- 1521-3773
- OpenAlex
- W1969240545
- Cited by
- 226
- References
- 1
- FWCI
- 17.66
- Type
- journal article
- Language
- en
- Open access
- closed
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- The paper
- Punna, S., Kuzelka, J., Wang, Q., & Finn, M. G. (2005). Head‐to‐Tail Peptide Cyclodimerization by Copper‐Catalyzed Azide–Alkyne Cycloaddition. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.200461656
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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.
