Tridentate complexes of 2,6-bis(4-substituted-1,2,3-triazol-1-ylmethyl) pyridine and its organic azide precursors: An application of the copper(II) acetate-accelerated azide-alkyne cycloaddition
Dalton Transactions, ISSN: 1477-9226, Vol: 40, Issue: 14, Page: 3655-3665
2011
- 46Citations
- 31Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations46
- Citation Indexes46
- CrossRef46
- 43
- Captures31
- Readers31
- 31
Article Description
Rapid coupling reactions between 2,6-bis(azidomethyl)pyridine and terminal alkynes in the presence of 5 mol% Cu(OAc)·HO without the addition of a reducing agent afford tridentate ligands for first-row transition-metal ions. The chelation between Cu and alkylated nitrogen atoms of the azido groups of 2,6-bis(azidomethyl)pyridine, as observed in the solid state, is credited for the acceleration of the azide-alkyne cycloaddition reactions. © The Royal Society of Chemistry 2011.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=79953836155&origin=inward; http://dx.doi.org/10.1039/c0dt01702g; http://www.ncbi.nlm.nih.gov/pubmed/21384008; https://xlink.rsc.org/?DOI=c0dt01702g; https://dx.doi.org/10.1039/c0dt01702g; https://pubs.rsc.org/en/content/articlelanding/2011/dt/c0dt01702g
Royal Society of Chemistry (RSC)
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