Evidence map›Paper›PMID 42557658›Full record

ArticleChemistry, an Asian journal2026

Ru(II)-Catalyzed Cascade Regioselective C-7 and C-8 Diamidation of Isoquinolinones Using Dioxazolones.

Ravichandran Manikandan, Annamalai Pratheepkumar

Abstract read
In one paragraph

Article in Chemistry, an Asian journal, 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

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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

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5 · Who and what money

Authors and funding

2 authors.

Ravichandran ManikandanDepartment of Chemistry, School of Advanced Sciences, Vellore Institute of Technology, Vellore, Tamil Nadu, India.
Annamalai PratheepkumarDepartment of Chemistry, School of Advanced Sciences, Vellore Institute of Technology, Vellore, Tamil Nadu, India.

Funding

DST-SERB, Anusandhan National Research Foundation (ANRF), India SRG/2023/002161Vellore Institute of Technology (VIT), Vellore SG20220089,SG20260162
6 · The paper itself

Abstract

In this study, we disclose an unprecedented ruthenium-catalyzed selective C-7 and C-8 diamidation of isoquinolinones via weak chelation assistance, employing dioxazolones as an efficient amidating agent. Significantly, in this reaction, dual C─H bonds were functionalized in one pot, enabling isoquinolinones embedded in diamidated scaffolds with high efficiency. The developed protocol enables the efficient synthesis of a broad array of diamidated isoquinolinones derivativities in excellent yields, including pharmaceutically relevant motifs derived from carboxylic acid and fatty acid containing dioxazolones. The resulting products exhibit excellent compatibility toward further synthetic diversification.

Indexed as

amidationdioxazolonesisoquinolinonesiterative C─H activationruthenium

Identifiers

PMID42557658
PMCPMC13443007

What OpenQuestion holds

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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.