Evidence map›Paper›PMID 40455572›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2025

Study on Phosphorus Compound/Catechol-Catalyzed Dehydrative Amidation and Its Database Development for Machine Learning.

Taiki Nagano, Dattatraya B Bagal, Ryuga Kunisada, Haruno Nakajima, Koki Sano, Naoki Noto, Susumu Saito

Abstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Taiki NaganoGraduate School of Science, Nagoya University, Nagoya, 464-8602, Japan.
Dattatraya B BagalResearch Center for Materials Science, Nagoya University, Nagoya, 464-8602, Japan.ORCID https://orcid.org/0000-0002-4755-5893
Ryuga KunisadaGraduate School of Science, Nagoya University, Nagoya, 464-8602, Japan.
Haruno NakajimaGraduate School of Science, Nagoya University, Nagoya, 464-8602, Japan.
Koki SanoGraduate School of Science, Nagoya University, Nagoya, 464-8602, Japan.
Naoki NotoIntegrated Research Consortium on Chemical Sciences (IRCCS), Nagoya University, Nagoya, 464-8602, Japan.ORCID https://orcid.org/0000-0003-0996-9160
Susumu SaitoIntegrated Research Consortium on Chemical Sciences (IRCCS) and Graduate School of Science, Nagoya University, Nagoya, 464-8602, Japan.ORCID https://orcid.org/0000-0003-0749-2020

Funding

Japan Science and Technology Agency JRMJCR22L2Japan Society for the Promotion of ScienceMEXT/JSPS Grants-in-aid for Transformative Research Areas (A) Digi-TOS, Early-Career Scientists 22H05356MEXT/JSPS Grants-in-aid for Transformative Research Areas (A) Digi-TOS, Early-Career Scientists 23K13744Transformative Research Areas (A) Green Catalysis, Specially Promoted Research, and International Leading Research, KAKENHI 22K21346Transformative Research Areas (A) Green Catalysis, Specially Promoted Research, and International Leading Research, KAKENHI 23H04904Transformative Research Areas (A) Green Catalysis, Specially Promoted Research, and International Leading Research, KAKENHI 23H05404
6 · The paper itself

Abstract

Herein, we report that the catalytic activity of phosphorus compounds with a P─H bond in dehydrative amidation reactions is substantially enhanced when using catechol derivatives as additives. A systematic investigation into the catalytic activity of four phosphorus compounds and 17 catechol derivatives allowed identifying several effective combinations, for example, dimethyl phosphite and 2,3-dihydroxynaphthalene, for the catalytic amidation of carboxylic acids with amines. The developed catalytic system enables the synthesis of pharmaceuticals and facilitates the amidation of anilines, which are typically considered poor substrates with low reactivity. In addition, machine-learning (ML) models were constructed to validate the effectiveness of the database generated from the above-mentioned investigation. Multilayer perceptron (MLP) models incorporating descriptors derived from both quantum chemical calculations and RDKit provided accurate predictions while maintaining chemical interpretability, which was underscored by a visual analysis using SHAP.

Indexed as

amidationcarboxylic acidsmachine learningphosphorus‐based catalysisSHAP

Identifiers

PMID40455572
PMCPMC12319358

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.