Synthesis of the tetracyclic skeleton of the lycopodium alkaloid lycopladine H via a pivotal double hydroformylation/intramolecular reductive amination sequence
Organic Letters, ISSN: 1523-7052, Vol: 17, Issue: 4, Page: 806-808
2015
- 13Citations
- 10Captures
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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
- Citations13
- Citation Indexes13
- 13
- CrossRef12
- Captures10
- Readers10
- 10
Article Description
A synthesis of the complete tetracyclic framework of the structurally unique Lycopodium alkaloid lycopladine H has been accomplished using a strategy involving a double alkene hydroformylation/intramolecular reductive amination to form the azocane and spiro-piperidine moieties of the natural product.
Bibliographic Details
American Chemical Society (ACS)
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