Visible light-induced aerobic oxidative cross-coupling of glycine esters with α-angelicalactone: a facile pathway to γ-lactams
Organic and Biomolecular Chemistry, ISSN: 1477-0520, Vol: 16, Issue: 36, Page: 6728-6734
2018
- 30Citations
- 6Captures
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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
- Citations30
- Citation Indexes30
- 30
- CrossRef24
- Captures6
- Readers6
Article Description
A metal-free aerobic oxidative dehydrogenative formal [2 + 3] cyclization of glycine esters with α-angelicalactone has been accomplished via the synergistic combination of photoredox catalysis and acid catalysis. This protocol provides straightforward and facile access to a series of substituted γ-lactams at room temperature under an air atmosphere. Moreover, the reaction could be carried out on a gram scale. The mild conditions as well as the use of cheap substrates and catalyst make this protocol very attractive for further synthetic applications.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85053715232&origin=inward; http://dx.doi.org/10.1039/c8ob01844h; http://www.ncbi.nlm.nih.gov/pubmed/30183788; https://xlink.rsc.org/?DOI=C8OB01844H; https://dx.doi.org/10.1039/c8ob01844h; https://pubs.rsc.org/en/content/articlelanding/2018/ob/c8ob01844h
Royal Society of Chemistry (RSC)
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