Synthesis of Cycloparaphenyleneacetylene via Alkyne Metathesis: C Complexation and Copper-Free Triple Click Reaction
Journal of the American Chemical Society, ISSN: 1520-5126, Vol: 138, Issue: 42, Page: 13814-13817
2016
- 64Citations
- 3Usage
- 56Captures
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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.
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Metrics Details
- Citations64
- Citation Indexes64
- CrossRef64
- 59
- Usage3
- Abstract Views3
- Captures56
- Readers56
- 56
Article Description
Alkyne metathesis provided an efficient macrocyclization route to a cycloparaphenyleneacetylene derivative in high yield. The cavity size was suitably matched for C which was tightly bound in an induced-fit fashion. The strained alkynes enabled a copper-free, 3-fold azide-alkyne cycloaddition at 50 °C.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84992695123&origin=inward; http://dx.doi.org/10.1021/jacs.6b08752; http://www.ncbi.nlm.nih.gov/pubmed/27723322; https://pubs.acs.org/doi/10.1021/jacs.6b08752; https://repository.lsu.edu/chemistry_pubs/681; https://repository.lsu.edu/cgi/viewcontent.cgi?article=1681&context=chemistry_pubs; https://digitalcommons.lsu.edu/chemistry_pubs/681; https://digitalcommons.lsu.edu/cgi/viewcontent.cgi?article=1681&context=chemistry_pubs
American Chemical Society (ACS)
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