Vinylogous and stereoselective domino synthesis of pyrano[2,3-c]pyrroles from alkylidene meldrum's acids
Organic and Biomolecular Chemistry, ISSN: 1477-0520, Vol: 22, Issue: 15, Page: 2948-2952
2024
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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
A domino Vinylogous aza-Michael-Aldol-Cyclocondensation (aza-VMAC) reaction was achieved with a series of alkylidene Meldrum's acid derivatives under simple operational conditions paving the way to novel pyrano[2,3-c]pyrroles in an excellent diasteroselectivity (>96 : 4), encompassing the relative control of three contiguous stereocenters.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85187706403&origin=inward; http://dx.doi.org/10.1039/d4ob00233d; http://www.ncbi.nlm.nih.gov/pubmed/38482880; https://xlink.rsc.org/?DOI=D4OB00233D; https://dx.doi.org/10.1039/d4ob00233d; https://pubs.rsc.org/en/content/articlelanding/2024/ob/d4ob00233d
Royal Society of Chemistry (RSC)
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