Applications of multicomponent reactions for the synthesis of diverse heterocyclic scaffolds
Organic Letters, ISSN: 1523-7060, Vol: 9, Issue: 21, Page: 4223-4226
2007
- 177Citations
- 22Captures
- 4Mentions
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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
- Citations177
- Citation Indexes177
- 177
- CrossRef158
- Captures22
- Readers22
- 22
- Mentions4
- References4
- Wikipedia4
Article Description
A four-component coupling process involving sequential reactions of aldehydes, primary amines, acid chlorides, and nucleophiles has been developed to prepare multifunctional substrates that may be employed in subsequent ring-forming reactions to generate a diverse array of functionalized heterocyclic scaffolds. This new approach to diversity-oriented synthesis was then applied to the first total synthesis of the isopavine alkaloid (±)-roelactamine. © 2007 American Chemical Society.
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