Evidence map›Paper›PMID 33087774›Full record

ArticleScientific reports2020

A new electrochemical strategy for the synthesis of a new type of sulfonamide derivatives.

Hamed Goljani, Zahra Tavakkoli, Ali Sadatnabi, Mahmood Masoudi-Khoram, Davood Nematollahi

Abstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
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  3. Article
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

5 authors.

Hamed GoljaniFaculty of Chemistry, Bu-Ali-Sina University, 65174-38683, Hamedan, Iran.
Zahra TavakkoliFaculty of Chemistry, Bu-Ali-Sina University, 65174-38683, Hamedan, Iran.
Ali SadatnabiFaculty of Chemistry, Bu-Ali-Sina University, 65174-38683, Hamedan, Iran.
Mahmood Masoudi-KhoramFaculty of Chemistry, Bu-Ali-Sina University, 65174-38683, Hamedan, Iran.
Davood NematollahiFaculty of Chemistry, Bu-Ali-Sina University, 65174-38683, Hamedan, Iran. nemat@basu.ac.ir.ORCID 0000-0001-9638-224X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study is the first report of electrochemical generation of hydroxyimino-cyclohexa-dien-ylidene haloniums and their application in the synthesis of new halo-N-hydroxysulfonamide derivatives. These compounds were obtained in a one-pot process based on the reaction of halonium acceptors with arylsulfinic acids. The method is easy to carry out, as it is performed using the carbon electrodes in a simple undivided cell. The protocol has a broad substrate scope with a tolerance for a variety of functional groups. The proposed mechanism is a ping-pong type reaction mechanism, which in its first stage the halonitroarene is reduced at the cathode to related hydroxylamine and in the second stage the cathodically generated hydroxylamine by oxidation at the anode and participating in disproportionation reaction is converted to the halonium acceptor.

Identifiers

PMID33087774
PMCPMC7577992

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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.