Enantioselective copper catalysed, direct functionalisation of allenes: Via allyl copper intermediates
Chemical Science, ISSN: 2041-6539, Vol: 8, Issue: 8, Page: 5240-5247
2017
- 103Citations
- 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
- Citations103
- Citation Indexes103
- CrossRef103
- 98
- Captures31
- Readers31
- 31
Review Description
The direct functionalisation of allenes under copper catalysis enables efficient access to enantioenriched, densely functionalised molecules. In this review we explore the breadth and depth of a versatile reaction manifold, which involves the element-cupration of allenes to generate allyl copper intermediates that are subsequently coupled with diverse arrays of electrophiles.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85026229568&origin=inward; http://dx.doi.org/10.1039/c7sc01968h; http://www.ncbi.nlm.nih.gov/pubmed/28959423; https://xlink.rsc.org/?DOI=C7SC01968H; http://xlink.rsc.org/?DOI=C7SC01968H; http://pubs.rsc.org/en/content/articlepdf/2017/SC/C7SC01968H; https://dx.doi.org/10.1039/c7sc01968h; https://pubs.rsc.org/en/content/articlelanding/2017/sc/c7sc01968h
Royal Society of Chemistry (RSC)
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