Evidence map›Paper›PMID 40733286›Full record

ReviewMolecules (Basel, Switzerland)2025

Advances in α-Arylation of Carbonyl Compounds: Diaryliodonium Salts as Arylating Agents.

Xiao-Wei Chen, Jia-Le Chen, Ling-Hui Zhang, Huhu Zhang, Xiaojun Chen, Xiaohui Fan

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

The trial behind it

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Xiao-Wei ChenSchool of Chemistry and Chemical Engineering, Lanzhou Jiaotong University, Lanzhou 730070, China.ORCID 0009-0009-2079-8105
Jia-Le ChenSchool of Chemistry and Chemical Engineering, Lanzhou Jiaotong University, Lanzhou 730070, China.
Ling-Hui ZhangState Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, China.
Huhu ZhangSchool of Chemistry and Chemical Engineering, Lanzhou Jiaotong University, Lanzhou 730070, China.
Xiaojun ChenAnimal Husbandry and Veterinary Bureau of Anding District, Dingxi 743021, China.
Xiaohui FanSchool of Chemistry and Chemical Engineering, Lanzhou Jiaotong University, Lanzhou 730070, China.

Funding

This project was supported by Gansu Provincial Science and Technology Program, Tianyou Youth Talent Lift Program of Lanzhou Jiaotong Universityand Young Scholars Science Foundation of Lanzhou Jiaotong University . Grant No. 25YFWA016; 24CXNJ013; 1520260514; 1200061308
6 · The paper itself

Abstract

Diaryliodonium salts are an important part of hypervalent iodine chemistry, owing to their highly electrophilic character, non-toxicity, and air and moisture stability, have been identified as an important arylating agent. It has been widely applied in the synthesis of natural products, drugs, and bioactive molecules bearing active α-arylation carbonyl units. Within the domain of α-arylation of carbonyl compounds using diaryliodonium salts, there is a notable absence in the literature of a comprehensive compilation dedicated to exclusive arylation processes involving these compounds. In this review, we focus on the overview of the recent advancements in utilizing diaryliodonium salts for α-arylation reactions, encompassing both racemic and asymmetric approaches to various carbonyl compounds including ketones, esters, enolates, and amides. Furthermore, we discuss the unique advantages and inherent limitations of diaryliodonium salts as arylating agents, as well as the underexplored application potentials that warrant further investigation in this rapidly evolving field.

Indexed as

arylating agentscarbonyl compoundsdiaryliodonium saltsα-arylation

Identifiers

PMID40733286
PMCPMC12299957

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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.