ArticleJournal of the American Chemical Society2017
Transition-Metal-Free Decarboxylative Iodination: New Routes for Decarboxylative Oxidative Cross-Couplings.
Article in Journal of the American Chemical Society, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
18 citing papers in PubMed.
- Regioselective synthesis of 3-halo-2Journal of pesticide science · 2026Article
- Deprotonation-controlled copper-free Pd-catalyzed Sonogashira couplingRSC advances · 2026Article
- Article
- Iodoarene Activation: Take a Leap Forward toward Green and Sustainable Transformations.Chemical reviews · 2025Review
- Formation of C(spJournal of the American Chemical Society · 2023Article
- New Approach to the Detection of Short-Lived Radical Intermediates.Journal of the American Chemical Society · 2022Article
- A Unified Approach to Decarboxylative Halogenation of (Hetero)aryl Carboxylic Acids.Journal of the American Chemical Society · 2022Article
- Palladium-Catalyzed Decarbonylative Iodination of Aryl Carboxylic Acids Enabled by Ligand-Assisted Halide Exchange.Angewandte Chemie (International ed. in English) · 2021Article
- Decarboxylative Halogenation of Organic Compounds.Chemical reviews · 2021Article
- One-step synthesis of benzo[Chemical science · 2020Article
- Palladium catalysed C-H arylation of pyrenes: access to a new class of exfoliating agents for water-based graphene dispersions.Chemical science · 2020Article
- Concerted Nucleophilic Aromatic Substitution Reactions.Angewandte Chemie (International ed. in English) · 2019Review
- Metathesis-active ligands enable a catalytic functional group metathesis between aroyl chlorides and aryl iodides.Nature chemistry · 2018Article
- Synthesis of Aryl Iodides from Arylhydrazines and Iodine.ACS omega · 2018Article
- Metal-free selective mono-halodecarboxylation of heteroarenes under mild conditions.Royal Society open science · 2018Article
- Transition-metal-free decarboxylative bromination of aromatic carboxylic acids.Chemical science · 2018Article
- Palladium- and Nickel-Catalyzed Decarbonylative C-S Coupling to Convert Thioesters to Thioethers.Organic letters · 2018Article
- Hypervalent iodine(III)-mediated decarboxylative acetoxylation at tertiary and benzylic carbon centers.Beilstein journal of organic chemistry · 2018Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Constructing products of high synthetic value from inexpensive and abundant starting materials is of great importance. Aryl iodides are essential building blocks for the synthesis of functional molecules, and efficient methods for their synthesis from chemical feedstocks are highly sought after. Here we report a low-cost decarboxylative iodination that occurs simply from readily available benzoic acids and I
Identifiers
What OpenQuestion holds
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.