ArticleOrganic letters2016
Lewis Acid Mediated Vinylogous Additions of Enol Nucleophiles into an α,β-Unsaturated Platinum Carbene.
Article in Organic letters, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
6 citing papers in PubMed.
- Last Decade of Unconventional Methodologies for the Synthesis of Substituted Benzofurans.Molecules (Basel, Switzerland) · 2020Review
- Regioselectivity Influences in Platinum-Catalyzed Intramolecular Alkyne O-H and N-H Additions.Organic letters · 2019Article
- Copper-catalyzed oxidative benzylic C-H cyclization via iminyl radical from intermolecular anion-radical redox relay.Nature communications · 2019Article
- Computational study of Ru-catalyzed cycloisomerization of 2-alkynylanilides.Journal of molecular modeling · 2018Article
- Platinum-Catalyzed α,β-Unsaturated Carbene Formation in the Formal Syntheses of Frondosin B and Liphagal.Organic letters · 2017Article
- C-C Bond Migration in the Cycloisomerization of 1,6-Enynes.Organic chemistry frontiers : an international journal of organic chemistry · 2016Article
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
A variety of substituted indoles and benzofurans are accessed via a platinum catalyzed annulation and vinylogous addition of enol nucleophiles. Several β-dicarbonyl compounds participate in the reaction, as do α-nitro and α-cyano carbonyl species. Subjecting the indole products to acidic conditions results in the formation of fused heterocycles.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.