Evidence map›Paper›PMID 42555390›Full record

ArticleRSC advances2026

Arenediazonium-generated aryl radical and nitrile coupling cascade under neat and catalyst-free conditions: green synthesis of anilides.

Qudrat Ullah, Waseem Ullah Khan, Rizwan Ullah, Tahira Bibi, Hammad Khan, Muhammad Israr, Aqsa, Abdullatif Bin Muhsinah, Rym Hassani, Muhammad Adil Ali and 3 more

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Article in RSC advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

13 authors.

Qudrat UllahOrganic Synthesis and Catalysis Research Laboratory, Institute of Chemical Sciences, University of Peshawar Peshawar 25120 Khyber Pakhtunkhwa Pakistan drshaukatali@uop.edu.pk.
Waseem Ullah KhanOrganic Synthesis and Catalysis Research Laboratory, Institute of Chemical Sciences, University of Peshawar Peshawar 25120 Khyber Pakhtunkhwa Pakistan drshaukatali@uop.edu.pk.
Rizwan UllahOrganic Synthesis and Catalysis Research Laboratory, Institute of Chemical Sciences, University of Peshawar Peshawar 25120 Khyber Pakhtunkhwa Pakistan drshaukatali@uop.edu.pk.
Tahira BibiOrganic Synthesis and Catalysis Research Laboratory, Institute of Chemical Sciences, University of Peshawar Peshawar 25120 Khyber Pakhtunkhwa Pakistan drshaukatali@uop.edu.pk.
Hammad KhanOrganic Synthesis and Catalysis Research Laboratory, Institute of Chemical Sciences, University of Peshawar Peshawar 25120 Khyber Pakhtunkhwa Pakistan drshaukatali@uop.edu.pk.
Muhammad IsrarCenter for Integrative Petroleum Research (CIPR), College of Petroleum Engineering and Geosciences, King Fahd University of Petroleum & Minerals Dhahran 31261 Saudi Arabia.
AqsaOrganic Synthesis and Catalysis Research Laboratory, Institute of Chemical Sciences, University of Peshawar Peshawar 25120 Khyber Pakhtunkhwa Pakistan drshaukatali@uop.edu.pk.
Abdullatif Bin MuhsinahDepartment of Pharmacognosy, College of Pharmacy, King Khalid University Abha 61441 Saudi Arabia.
Rym HassaniEnvironment and Nature Research Centre, Jazan University P. O. Box 114 Jazan 45142 Saudi Arabia.
Muhammad Adil AliOrganic Synthesis and Catalysis Research Laboratory, Institute of Chemical Sciences, University of Peshawar Peshawar 25120 Khyber Pakhtunkhwa Pakistan drshaukatali@uop.edu.pk.
Ajmal KhanNatural and Medical Sciences Research Center, University of Nizwa P. O. Box 33, 616 Birkat Al Mauz Nizwa Oman ajmalkhan@unizwa.edu.om.
Syed Adnan Ali ShahFaculty of Pharmacy, Universiti Teknologi MARA (UiTM) Cawangan Selangor Kampus Puncak Alam Bandar Puncak Alam 42300 Selangor Darul Ehsan Malaysia syedadnan@uitm.edu.my.
Shaukat AliOrganic Synthesis and Catalysis Research Laboratory, Institute of Chemical Sciences, University of Peshawar Peshawar 25120 Khyber Pakhtunkhwa Pakistan drshaukatali@uop.edu.pk.ORCID https://orcid.org/0000-0002-5915-3787

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In addition to their use as building blocks in organic synthesis, anilides are widely applied in a variety of industries, such as pharmaceutical, materials science, and agrochemical. The previously reported methods generally require transition-metal catalysts, co-catalysts, bases, solvents, and additives. Herein, we report a neat, catalyst-, and additive-free sustainable method for generating aryl radicals from arenediazonium salts and their subsequent reactions with nitriles to afford anilides under mild conditions (80 °C). The reaction features promising green chemistry metrics, including a low

Identifiers

PMID42555390
PMCPMC13370580

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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.