Evidence map›Paper›PMID 34199620›Full record

ArticleMolecules (Basel, Switzerland)2021

Synthesis of 4-Substituted-1,2-Dihydroquinolines by Means of Gold-Catalyzed Intramolecular Hydroarylation Reaction of

Antonio Arcadi, Andrea Calcaterra, Giancarlo Fabrizi, Andrea Fochetti, Antonella Goggiamani, Antonia Iazzetti, Federico Marrone, Vincenzo Marsicano, Giulia Mazzoccanti, Andrea Serraiocco

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2021. 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

10 authors.

Antonio ArcadiDipartimento di Scienze Fisiche e Chimiche, Università degli Studi di L'Aquila, 67100 Coppito, Italy.ORCID 0000-0001-9053-648X
Andrea CalcaterraDipartimento di Chimica e Tecnologie del Farmaco, Dipartimento di Eccellenza 2018-2022, Sapienza Università di Roma, 00185 Rome, Italy.ORCID 0000-0001-7036-6620
Giancarlo FabriziDipartimento di Chimica e Tecnologie del Farmaco, Dipartimento di Eccellenza 2018-2022, Sapienza Università di Roma, 00185 Rome, Italy.
Andrea FochettiDipartimento di Chimica e Tecnologie del Farmaco, Dipartimento di Eccellenza 2018-2022, Sapienza Università di Roma, 00185 Rome, Italy.
Antonella GoggiamaniDipartimento di Chimica e Tecnologie del Farmaco, Dipartimento di Eccellenza 2018-2022, Sapienza Università di Roma, 00185 Rome, Italy.
Antonia IazzettiDipartimento di Chimica e Tecnologie del Farmaco, Dipartimento di Eccellenza 2018-2022, Sapienza Università di Roma, 00185 Rome, Italy.
Federico MarroneDipartimento di Chimica e Tecnologie del Farmaco, Dipartimento di Eccellenza 2018-2022, Sapienza Università di Roma, 00185 Rome, Italy.
Vincenzo MarsicanoDipartimento di Scienze Fisiche e Chimiche, Università degli Studi di L'Aquila, 67100 Coppito, Italy.ORCID 0000-0003-4028-4370
Giulia MazzoccantiDipartimento di Chimica e Tecnologie del Farmaco, Dipartimento di Eccellenza 2018-2022, Sapienza Università di Roma, 00185 Rome, Italy.ORCID 0000-0001-8655-524X
Andrea SerraioccoDipartimento di Chimica e Tecnologie del Farmaco, Dipartimento di Eccellenza 2018-2022, Sapienza Università di Roma, 00185 Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An alternative Au(I)-catalyzed synthetic route to functionalized 1,2-dihydroquinolines is reported. This novel approach is based on the use of

Indexed as

1,2-dihydroquinolinesgold catalysisintramolecular hydroarylation

Identifiers

PMID34199620
PMCPMC8199670

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.