An enantioselective synthesis of α-alkylated pyrroles: Via cooperative isothiourea/palladium catalysis
Organic and Biomolecular Chemistry, ISSN: 1477-0520, Vol: 17, Issue: 7, Page: 1787-1790
2019
- 32Citations
- 14Captures
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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
- Citations32
- Citation Indexes32
- CrossRef32
- 29
- Captures14
- Readers14
- 14
Article Description
Herein we describe the direct enantioselective Lewis base/Pd catalysed α-allylation of pyrrole acetic acid esters. This provides high isolated yields of highly enantioenriched products and exhibits broad reaction scope with respect to both reaction partners. The products can be readily elaborated in a manner which points towards potential applications in target directed synthesis.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85061503365&origin=inward; http://dx.doi.org/10.1039/c8ob02600a; http://www.ncbi.nlm.nih.gov/pubmed/30483696; https://xlink.rsc.org/?DOI=C8OB02600A; https://dx.doi.org/10.1039/c8ob02600a; https://pubs.rsc.org/en/content/articlelanding/2019/ob/c8ob02600a
Royal Society of Chemistry (RSC)
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