NBS-promoted oxidation of fullerene monoradicals leading to regioselective 1,4-difunctional fullerenes
Chemical Communications, ISSN: 1364-548X, Vol: 50, Issue: 99, Page: 15730-15732
2014
- 14Citations
- 6Captures
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Metrics Details
- Citations14
- Citation Indexes14
- CrossRef14
- 14
- Captures6
- Readers6
Article Description
We have demonstrated that NBS is able to promote the oxidation of fullerene monoradicals to form 1,4-difunctional fullerenes. The singly bonded fullerene dimers were used as fullerene monoradical precursors, which produced various 1,4-fullerenes with a wide range of functional groups in good to high yields with high regioselectivity in terms of cosolvents and nucleophiles. © The Royal Society of Chemistry 2014.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84911480002&origin=inward; http://dx.doi.org/10.1039/c4cc07780f; http://www.ncbi.nlm.nih.gov/pubmed/25364795; https://xlink.rsc.org/?DOI=C4CC07780F; http://xlink.rsc.org/?DOI=C4CC07780F; http://pubs.rsc.org/en/content/articlepdf/2014/CC/C4CC07780F; https://dx.doi.org/10.1039/c4cc07780f; https://pubs.rsc.org/en/content/articlelanding/2014/cc/c4cc07780f
Royal Society of Chemistry (RSC)
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