Evidence map›Paper›PMID 42163798›Full record

ReviewChemical record (New York, N.Y.)2026

Catalytic Transformations of Aza-Cyclobutenes, Fused Cyclobutenes, and Cyclobutenones.

Asad Aziz, Zhanhui Yang

Abstract readReview
In one paragraph

Review in Chemical record (New York, N.Y.), 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

2 authors.

Asad AzizCollege of Chemistry, Beijing University of Chemical Technology, Beijing, P. R. China.
Zhanhui YangCollege of Chemistry, Beijing University of Chemical Technology, Beijing, P. R. China.ORCID https://orcid.org/0000-0001-7050-8780

Funding

Fundamental Research Funds for the Central Universities of Beijing University of Chemical Technology PY25215National Natural Science Foundation of China 22371011Natural Science Foundation of Beijing Municipality 2252016
6 · The paper itself

Abstract

Cyclobutenes, four-membered cyclic compounds with a carbon-carbon double bond, are valuable intermediates in organic synthesis, offering unique reactivity due to their ring strain. This review focuses on three major types including aza-cyclobutene, fused cyclobutene, and cyclobutenone, highlighting their synthetic versatility and reactivity. Aza-cyclobutenes enable diverse functionalization strategies for constructing complex N-heterocyclic structures. Fused cyclobutenes with their bicyclic nature are explored for applications in stereoselective chemical transformations, polymer, and materials science, while cyclobutenones, with their electrophilic carbonyl group, serve as key intermediates in polyfunctionalized frameworks. We discuss recent advancements in catalysis, including transition metal- and photoredox-mediated transformations, which enable selective, enantioselective, and regioselective reactions. The review also addresses emerging challenges and future directions, emphasizing the scalability of these methods for industrial applications. This comprehensive overview underscores the transformative potential of cyclobutenes in synthetic organic chemistry.

Indexed as

2‐azetinecyclobutenescyclobutenoneselectrocyclic ring openingfused cyclobutenes

Identifiers

PMID42163798
PMCPMC13480828

What OpenQuestion holds

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Registered trials

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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.