Evidence map›Paper›PMID 41552476›Full record

ArticleACS omega2026

Sequential Formal (4 + 1)-Spirocycloaddition/Oxidative Cleavage between Indoles and

Nikolai A Arutiunov, Anna M Zatsepilina, Kirill V Tolstov, Daria A Shtal, Nicolai A Aksenov, Alexander V Aksenov

Abstract read
In one paragraph

Article in ACS omega, 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

6 authors.

Nikolai A ArutiunovDepartment of Chemistry, North Caucasus Federal University, 1a Pushkin St., Stavropol 355009, Russian Federation.ORCID https://orcid.org/0000-0003-2675-9093
Anna M ZatsepilinaDepartment of Chemistry, North Caucasus Federal University, 1a Pushkin St., Stavropol 355009, Russian Federation.
Kirill V TolstovDepartment of Chemistry, North Caucasus Federal University, 1a Pushkin St., Stavropol 355009, Russian Federation.
Daria A ShtalDepartment of Chemistry, North Caucasus Federal University, 1a Pushkin St., Stavropol 355009, Russian Federation.
Nicolai A AksenovDepartment of Chemistry, North Caucasus Federal University, 1a Pushkin St., Stavropol 355009, Russian Federation.ORCID https://orcid.org/0000-0002-7125-9066
Alexander V AksenovDepartment of Chemistry, North Caucasus Federal University, 1a Pushkin St., Stavropol 355009, Russian Federation.ORCID https://orcid.org/0000-0002-6644-9949

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An effective protocol for the synthesis of benzamide-containing (3),4,5-substituted isoxazoles was developed. This one-pot procedure involved a formal (4 + 1)-spirocycloaddition between indoles and β-nitrostyrenes, followed by an oxidative cleavage with a mixture of acetic anhydride and hydrogen peroxide, which led to the formation of a highly functionalized isoxazole moiety. A total of 33 such compounds were synthesized in yields ranging from 44% to 91%, demonstrating good tolerance for various functional groups.

Identifiers

PMID41552476
PMCPMC12809815

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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.