ReviewChemical science2021
Recent discoveries on the structure of iodine(iii) reagents and their use in cross-nucleophile coupling.
Review in Chemical science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 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
22 citing papers in PubMed.
- Pushing C-N bond formation in water: sustainable strategies, mechanistic roles and future perspectives.RSC advances · 2026Review
- Structural Tuning of InefficientACS omega · 2026Article
- Catalytic Enantioselective Cross-Nucleophile Coupling via Valence Tautomerism.Journal of the American Chemical Society · 2025Article
- Synthesis of 2,2-Disubstituted Indolin-3-ones via Enolonium Species.The Journal of organic chemistry · 2025Article
- Iodoarene Activation: Take a Leap Forward toward Green and Sustainable Transformations.Chemical reviews · 2025Review
- Recent Progress in Synthetic Applications of Hypervalent Iodine(III) Reagents.Chemical reviews · 2024Review
- Silver-Catalyzed (Journal of the American Chemical Society · 2024Article
- Diaryl hypervalent bromines and chlorines: synthesis, structures and reactivities.Chemical science · 2024Review
- Iodoxybenzoic Acid (IBX) in Organic Synthesis: A Septennial Review.Current organic synthesis · 2024Article
- Lewis Base-assisted Arylation of Unsaturated Carbonyls.Chemistry (Weinheim an der Bergstrasse, Germany) · 2023Article
- New Strategies for the Functionalization of Carbonyl Derivatives via α-Umpolung: From Enolates to Enolonium Ions.Accounts of chemical research · 2023Article
- 2-Fluoroenones via an Umpolung Morita-Baylis-Hillman Reaction of Enones.Organic letters · 2023Article
- Structure Elucidation of In Situ Generated Chiral Hypervalent Iodine Complexes via Vibrational Circular Dichroism (VCD).Angewandte Chemie (International ed. in English) · 2022Article
- Synthesis of Cyclic and Acyclic ortho-Aryloxy Diaryliodonium Salts for Chemoselective Functionalizations.Chemistry (Weinheim an der Bergstrasse, Germany) · 2022Article
- α-Thianthrenium Carbonyl Species: The Equivalent of an α-Carbonyl Carbocation.Angewandte Chemie (International ed. in English) · 2022Article
- An Expedient Method for the Umpolung Coupling of Enols with Heteronucleophiles.Chemistry (Weinheim an der Bergstrasse, Germany) · 2022Article
- Orbital analysis of bonding in diarylhalonium salts and relevance to periodic trends in structure and reactivity.Chemical science · 2022Article
- Sulfur(iv)-mediated umpolung α-heterofunctionalization of 2-oxazolines.Chemical science · 2022Article
- Article
- Exploring benzylicChemical science · 2021Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
Abstract
This perspective article discusses structural features of iodine(iii) compounds as a prelude to presenting their use as umpolung reagents, in particular as pertains to their ability to promote the selective coupling of two nucleophilic species
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.