BINEPINES: Chiral binaphthalene-core monophosphepine ligands for multipurpose asymmetric catalysis
Chemical Society Reviews, ISSN: 1460-4744, Vol: 40, Issue: 7, Page: 3744-3763
2011
- 64Citations
- 39Captures
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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
- 64
- CrossRef62
- Captures39
- Readers39
- 39
Article Description
The atropisomeric structure of 4,5-dihydro-3H-dinaphtho[2,1-c;1′,2′e]phosphepine is the common axially chiral scaffold of a library of monophosphine ligands nicknamed BINEPINES that have shown a quite remarkable stereoselection efficiency in a broad variety of enantioselective reactions involving the formation of new C–H or C–C or C–X bonds. In this critical review the properties and scope of this type of chiral ligands are illustrated (70 references). © 2011 The Royal Society of Chemistry.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=79959399753&origin=inward; http://dx.doi.org/10.1039/c0cs00164c; http://www.ncbi.nlm.nih.gov/pubmed/21547309; https://xlink.rsc.org/?DOI=c0cs00164c; https://dx.doi.org/10.1039/c0cs00164c; https://pubs.rsc.org/en/content/articlelanding/2011/cs/c0cs00164c
Royal Society of Chemistry (RSC)
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