The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Metal‐Free Triazole Formation as a Tool for Bioconjugation
Abstract
Who needs copper? There is a strong demand for ligation reactions that proceed spontaneously, selectively, and under physiological conditions. To meet these criteria, we used trifluoromethyl-substituted oxanorbornadienes in reactions with various azides, and achieved an elegant tandem [3+2] cycloaddition–retro-Diels–Alder reaction that forms stable 1,2,3-triazole-linked bioconjugates (see scheme).
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Tornøe, C. W., Christensen, C., & Meldal, M. (2002) · The Journal of Organic Chemistry · doi:10.1021/jo011148j · Cited by 8,696
Effect of pegylation on pharmaceuticals
Harris, J. M., & Chess, R. B. (2003) · Nature Reviews Drug Discovery · doi:10.1038/nrd1033 · Cited by 3,431
RGD AND OTHER RECOGNITION SEQUENCES FOR INTEGRINS
Ruoslahti, E. (1996) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.12.1.697 · Cited by 3,191
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
Cited by
Bioorthogonal Chemistry: Fishing for Selectivity in a Sea of Functionality
Sletten, E. M., & Bertozzi, C. R. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200900942 · Cited by 3,165
Cu-free click cycloaddition reactions in chemical biology
Jewett, J. C., & Bertozzi, C. R. (2010) · Chemical Society Reviews · doi:10.1039/b901970g · Cited by 1,684
Cellular Incorporation of Unnatural Amino Acids and Bioorthogonal Labeling of Proteins
Lang, K., & Chin, J. W. (2014) · Chemical Reviews · doi:10.1021/cr400355w · Cited by 1,035
Ning, X., Guo, J., Wolfert, M. A., & Boons, G. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200705456 · Cited by 924
Click Chemistry beyond Metal‐Catalyzed Cycloaddition
Becer, C. R., Hoogenboom, R., & Schubert, U. S. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200900755 · Cited by 866
Metadata
- Authors
- van Berkel, S. S., Dirks, A. (. J., Debets, M. F., van Delft, F. L., Cornelissen, J. J. L. M., Nolte, R. J. M., & Rutjes, F. P. J. T.
- Venue
- ChemBioChem
- Publisher
- Wiley
- Published
- 2007-08-27
- Volume
- 8
- Issue
- 13
- Pages
- 1504-1508
- ISSN
- 1439-4227 (ISSN-L)
- 1439-7633
- OpenAlex
- W2110615697
- Cited by
- 201
- References
- 4
- FWCI
- 9.47
- Type
- journal article
- Language
- en
- Open access
- closed
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- van Berkel, S. S., Dirks, A. (. J., Debets, M. F., van Delft, F. L., Cornelissen, J. J. L. M., Nolte, R. J. M., & Rutjes, F. P. J. T. (2007). Metal‐Free Triazole Formation as a Tool for Bioconjugation. ChemBioChem. https://doi.org/10.1002/cbic.200700278
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