Evidence map›Paper›PMID 42429134›Full record

ArticleAngewandte Chemie (International ed. in English)2026

Conversion of Alkenes Into Simple or Functionalized Aldehydes by Reaction With an Ambiphilic Masked Formyl Radical.

Sheng-Qiang Lai, Peng-Fei Zhao, Zuo-Shuai Wang, Hong-Chen Wang, Xiao-Jian Wang, Lin-Yuan Zhu, Bing Han

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Angewandte Chemie (International ed. in English), 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

7 authors.

Sheng-Qiang LaiState Key Laboratory of Natural Product Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, China.
Peng-Fei ZhaoState Key Laboratory of Natural Product Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, China.
Zuo-Shuai WangState Key Laboratory of Natural Product Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, China.
Hong-Chen WangState Key Laboratory of Natural Product Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, China.
Xiao-Jian WangState Key Laboratory of Natural Product Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, China.
Lin-Yuan ZhuState Key Laboratory of Natural Product Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, China.
Bing HanState Key Laboratory of Natural Product Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, China.ORCID https://orcid.org/0000-0003-0507-9742

Funding

National Natural Science Foundation of China 22171118National Natural Science Foundation of China 22471109Science and Technology Major Program of Gansu Province of China 22ZD6FA006Science and Technology Major Program of Gansu Province of China 23ZDFA015Science and Technology Major Program of Gansu Province of China 24ZD13FA017
6 · The paper itself

Abstract

The synthetic application of formyl radicals and other masked formyl radicals is constrained by their weak electrophilicity (ω = 1.17 eV for the formyl radical, ω = 0.58 eV for the •CH(OEt)

Indexed as

aldehydesalkenesambiphilicformylationradical reactions

Identifiers

PMID42429134
PMCPMC13573096

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.