Evidence map›Paper›PMID 42899083›Full record

ReviewBeilstein journal of organic chemistry2026

Mechanochemical synthesis using hypervalent iodine reagents.

Nasser Amri

Abstract readReview
In one paragraph

Review in Beilstein journal of organic chemistry, 2026. 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

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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

1 author.

Nasser AmriDepartment of Physical Sciences, Chemistry Division, College of Science, Jazan University, P.O. Box 114, Jizan 45142, Saudi Arabia.ORCID https://orcid.org/0000-0002-7971-2275

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mechanochemical activation offers a powerful means of expanding the reactivity of hypervalent iodine reagents while advancing solvent-free synthetic methodologies. This review surveys the evolution of iodine(III) and iodine(V) chemistry in the solid state, from foundational solvent-free oxidations to mechanochemical approaches that enable efficient heterocycle construction, C-H functionalization, cascade dioxygenation, fluoroiodane-mediated fluorocyclization, and redox-initiated polymerization. Mechanical energy alters aggregation, enhances reagent-substrate contact, and promotes transformation pathways not readily accessible in solution. These developments showcase the distinctive advantages of mechanochemical hypervalent iodine chemistry and its growing impact on sustainable synthetic methodology development.

Indexed as

heterocycleshypervalent iodinemechanochemistryoxidative functionalizationpolymerization

Identifiers

PMID42899083
PMCPMC13678683

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.