Evidence map›Paper›PMID 33233747›Full record

ReviewMolecules (Basel, Switzerland)2020

Recent Advances in One-Pot Modular Synthesis of 2-Quinolones.

Wan Pyo Hong, Inji Shin, Hee Nam Lim

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Organocatalytic Electrophilic Arene Amination: Rapid Synthesis of 2-Quinolones.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025
    Article
  6. Therapeutic Potental of Quinolin-2Mini reviews in medicinal chemistry · 2025
    Review
  7. Article
  8. Review
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

3 authors.

Wan Pyo HongSchool of Advanced Materials and Chemical Engineering, Daegu Catholic University, 13-13, Hayang-ro, Hayang-eup, Gyeongsan-si, Gyeongbuk 38430, Korea.
Inji ShinDepartment of Fine Chemistry, Seoul National University of Science and Technology, 232 Gongneung-ro, Nowon-gu, Seoul 01811, Korea.ORCID 0000-0002-8165-6276
Hee Nam LimEco-Friendly New Materials Research Center, Therapeutics&Biotechnology Division, 141, Gajeong-ro, Yuseong-gu, Daejeon 34114, Korea.

Funding

National Research Foundation of Korea NRF2019R1C1C1004970National Research Foundation of Korea NRF2019R1C1C1005737National Research Foundation of Korea NRF2020R1I1A3071821
6 · The paper itself

Abstract

It is known that 2-quinolones are broadly applicable chemical structures in medicinal and agrochemical research as well as various functional materials. A number of current publications about their synthesis and their applications emphasize the importance of these small molecules. The early synthetic chemistry originated from the same principle of the classical Friedländer and Knorr procedures for the preparation of quinolines. The analogous processes were developed by applying new synthetic tools such as novel catalysts, the microwave irradiation method, etc., whereas recent innovations in new bond forming reactions have allowed for novel strategies to construct the core structures of 2-quinolones beyond the bond disconnections based on two classical reactions. Over the last few decades, some reviews on structure-based, catalyst-based, and bioactivity-based studies have been released. In this focused review, we extensively surveyed recent examples of one-pot reactions, particularly in view of modular approaches. Thus, the contents are categorized as three major sections (two-, three-, and four-component reactions) according to the number of reagents that ultimately compose atoms of the core structures of 2-quinolones. The collected synthetic methods are discussed from the perspectives of strategy, efficiency, selectivity, and reaction mechanism.

Indexed as

Chemistry Techniques, SyntheticCatalysisHydroxyquinolinesMetalsMolecular StructureQuinolonescarbostyrilHydroxyquinolinesMetalsQuinolones2-quinolonecascadecatalysisdrugmulti-componentN-heterocycleone-pot

Identifiers

PMID33233747
PMCPMC7699938

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Registered trials

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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.