ArticleEuropean journal of organic chemistry2016
Photocatalytic Aminodecarboxylation of Carboxylic Acids.
Article in European journal of organic chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
What it found
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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
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Who cites it
8 citing papers in PubMed.
- Development of N-centered radical scavengers that enables photoredox-catalyzed transition-metal-free radical amination of alkyl pinacol boronates.Nature communications · 2025Article
- Direct catalytic photodecarboxylative amination of carboxylic acids with diazirines for divergent access to nitrogen-containing compounds.Cell reports. Physical science · 2024Article
- Radical Decarboxylative Carbon-Nitrogen Bond Formation.Molecules (Basel, Switzerland) · 2023Review
- Recent advances in visible light-induced C(Nature reviews. Chemistry · 2022Article
- Generation of Alkyl Radicals: From the Tyranny of Tin to the Photon Democracy.Chemical reviews · 2020Article
- Nickel-catalyzed decarbonylation ofChemical science · 2019Article
- Decarboxylative hydrazination of unactivated carboxylic acids by cerium photocatalysis.Chemical communications (Cambridge, England) · 2019Article
- Photoinduced, Copper-Catalyzed Decarboxylative C-N Coupling to Generate Protected Amines: An Alternative to the Curtius Rearrangement.Journal of the American Chemical Society · 2017Article
Corrections and comments
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Authors and funding
5 authors.
Funding
Abstract
Aminodecarboxylation of unactivated alkyl carboxylic acids has been accomplished utilizing an organic photocatalyst. This operationally simple reaction utilizes readily available carboxylic acids to chemoselectively generate reactive alkyl intermediates that are not accessible via conventional two-electron pathways. The organic radical intermediates are efficiently trapped with electrophilic diazo compounds to provide aminated alkanes.
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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.