The DOI matches its Crossref record; 26 of the 26 references it cites were found in a registry or an index.
Click Chemistry: Copper Clusters Catalyse the Cycloaddition of Azides with Terminal Alkynes
Abstract
Air‐stable copper nanoclusters are good catalysts in the Cu(I)‐catalysed “click” cycloaddition of azides with terminal alkynes to give 1,4‐disubstituted 1,2,3‐triazoles. No additional base or reducing agent is required. The reaction kinetics using various copper catalyst types and the function of copper particles in this system are studied and discussed.
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Cites
Tornøe, C. W., Christensen, C., & Meldal, M. (2002) · The Journal of Organic Chemistry · doi:10.1021/jo011148j · Cited by 8,696
Sonogashira, K., Tohda, Y., & Hagihara, N. (1975) · Tetrahedron Letters · doi:10.1016/s0040-4039(00)91094-3 · Cited by 5,208
The growing impact of click chemistry on drug discovery
Kolb, H. C., & Sharpless, K. B. (2003) · Drug Discovery Today · doi:10.1016/s1359-6446(03)02933-7 · Cited by 3,148
Metal‐Catalyzed Cross‐Coupling Reactions
(1998) · Wiley eBooks · doi:10.1002/9783527612222 · Cited by 2,529
Himo, F., Lovell, T., Hilgraf, R., Rostovtsev, V. V., Noodleman, L., Sharpless, K. B., & Fokin, V. V. (2005) · Journal of the American Chemical Society · doi:10.1021/ja0471525 · Cited by 1,738
Bioconjugation by Copper(I)-Catalyzed Azide-Alkyne [3 + 2] Cycloaddition
Wang, Q., Chan, T. R., Hilgraf, R., Fokin, V. V., Sharpless, K. B., & Finn, M. G. (2003) · Journal of the American Chemical Society · doi:10.1021/ja021381e · Cited by 1,641
Acetylenic Coupling: A Powerful Tool in Molecular Construction
Siemsen, P., Livingston, R. C., & Diederich, F. (2000) · Angewandte Chemie International Edition · doi:10.1002/1521-3773(20000804)39:15<2632::aid-anie2632>3.0.co;2-f · Cited by 1,535
Polytriazoles as Copper(I)-Stabilizing Ligands in Catalysis
Chan, T. R., Hilgraf, R., Sharpless, K. B., & Fokin, V. V. (2004) · Organic Letters · doi:10.1021/ol0493094 · Cited by 1,531
Wu, P., Feldman, A. K., Nugent, A. K., Hawker, C. J., Scheel, A., Voit, B., Pyun, J., Fréchet, J. M. J., Sharpless, K. B., & Fokin, V. V. (2004) · Angewandte Chemie International Edition · doi:10.1002/anie.200454078 · Cited by 1,167
Narayanan, R., & El-Sayed, M. A. (2003) · Journal of the American Chemical Society · doi:10.1021/ja035044x · Cited by 779
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
“Click”‐Chemistry in Polymer and Material Science: the Update
Binder, W. H. (2008) · Macromolecular Rapid Communications · doi:10.1002/marc.200800332 · Cited by 567
Cu(I)-Catalyzed Click Chemistry in Glycoscience and Their Diverse Applications
Agrahari, A. K., Bose, P., Jaiswal, M. K., Rajkhowa, S., Singh, A. S., Hotha, S., Mishra, N., & Tiwari, V. K. (2021) · Chemical Reviews · doi:10.1021/acs.chemrev.0c00920 · Cited by 445
Transition‐metal nanoparticles: synthesis, stability and the leaching issue
Pachón, L. D., & Rothenberg, G. (2008) · Applied Organometallic Chemistry · doi:10.1002/aoc.1382 · Cited by 443
Self-citationMetal chelating systems synthesized using the copper(i) catalyzed azide-alkynecycloaddition
Struthers, H., Mindt, T. L., & Schibli, R. (2010) · Dalton Trans. · doi:10.1039/b912608b · Cited by 386
Metadata
- Authors
- Pachón, L. D., van Maarseveen, J. H., & Rothenberg, G.
- Venue
- Advanced Synthesis & Catalysis
- Publisher
- Wiley
- Published
- 2005-05
- Volume
- 347
- Issue
- 6
- Pages
- 811-815
- ISSN
- 1615-4150 (ISSN-L)
- 1615-4169
- OpenAlex
- W2156484600
- Cited by
- 285
- References
- 26
- FWCI
- 8.73
- Type
- journal article
- Language
- en
- Open access
- closed
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- Pachón, L. D., van Maarseveen, J. H., & Rothenberg, G. (2005). Click Chemistry: Copper Clusters Catalyse the Cycloaddition of Azides with Terminal Alkynes. Advanced Synthesis & Catalysis. https://doi.org/10.1002/adsc.200404383
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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.