A reusable polymer anchored pyridine mediated formal [4 + 1] annulation reaction for the diastereoselective synthesis of 2,3-dihydrobenzofurans
Organic and Biomolecular Chemistry, ISSN: 1477-0520, Vol: 21, Issue: 27, Page: 5542-5546
2023
- 7Citations
- 2Captures
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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.
Article Description
We have developed a highly stereoselective formal [4 + 1] annulation reaction to construct trans-2,3-dihydrobenzofurans utilising in situ generated supported pyridinium ylide. This approach has excellent substrate versatility and gram-scale synthesis capability. Moreover, the polymer-anchored pyridine has been recovered and reused multiple times. The product has been transformed into valuable molecules.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85164302474&origin=inward; http://dx.doi.org/10.1039/d3ob00804e; http://www.ncbi.nlm.nih.gov/pubmed/37376919; https://xlink.rsc.org/?DOI=D3OB00804E; https://dx.doi.org/10.1039/d3ob00804e; https://pubs.rsc.org/en/content/articlelanding/2023/ob/d3ob00804e
Royal Society of Chemistry (RSC)
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