Evidence map›Paper›PMID 30344776›Full record

ArticleBeilstein journal of organic chemistry2018

Quinolines from the cyclocondensation of isatoic anhydride with ethyl acetoacetate: preparation of ethyl 4-hydroxy-2-methylquinoline-3-carboxylate and derivatives.

Nicholas G Jentsch, Jared D Hume, Emily B Crull, Samer M Beauti, Amy H Pham, Julie A Pigza, Jacques J Kessl, Matthew G Donahue

Open access · diamondAbstract read
In one paragraph

Article in Beilstein journal of organic chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 19% of its field
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

9 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Scalable Preparation of the Masked Acyl Cyanide TBS-MAC.Molecules (Basel, Switzerland) · 2023
    Article
  7. Article
  8. Review
  9. 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

8 authors at 1 institution in 1 country.

Nicholas G JentschDepartment of Chemistry and Biochemistry, University of Southern Mississippi, 118 College Drive #5043, Hattiesburg, MS 39406, USA.ORCID 0000-0001-8264-9222
Jared D HumeDepartment of Chemistry and Biochemistry, University of Southern Mississippi, 118 College Drive #5043, Hattiesburg, MS 39406, USA.ORCID 0000-0002-0214-3190
Emily B CrullDepartment of Chemistry and Biochemistry, University of Southern Mississippi, 118 College Drive #5043, Hattiesburg, MS 39406, USA.ORCID 0000-0003-3839-7579
Samer M BeautiDepartment of Chemistry and Biochemistry, University of Southern Mississippi, 118 College Drive #5043, Hattiesburg, MS 39406, USA.ORCID 0000-0003-0844-7686
Amy H PhamDepartment of Chemistry and Biochemistry, University of Southern Mississippi, 118 College Drive #5043, Hattiesburg, MS 39406, USA.ORCID 0000-0002-0969-6679
Julie A PigzaDepartment of Chemistry and Biochemistry, University of Southern Mississippi, 118 College Drive #5043, Hattiesburg, MS 39406, USA.ORCID 0000-0002-1289-5679
Jacques J KesslDepartment of Chemistry and Biochemistry, University of Southern Mississippi, 118 College Drive #5043, Hattiesburg, MS 39406, USA.ORCID 0000-0001-8103-6678
Matthew G DonahueDepartment of Chemistry and Biochemistry, University of Southern Mississippi, 118 College Drive #5043, Hattiesburg, MS 39406, USA.ORCID 0000-0002-2608-1529
University of Southern Mississippi · US

Funding

Training and Mentoring Core P20GM103476 · NIGMS · UNIVERSITY OF SOUTHERN MISSISSIPPI · PI MICHAEL R GARRETT · 2012 to 2026
$60.2M
Asymmetric Synthesis of Bioactive Nitrogen HeterocyclesR15GM129751 · NIGMS · UNIVERSITY OF SOUTHERN MISSISSIPPI · PI DONAHUE, MATTHEW GARRETT · 2018 to 2018
$439k
Mode of Action of Allosteric HIV-1 Integrase Inhibitors during Late Steps of Viral ReplicationR21AI127282 · NIAID · UNIVERSITY OF SOUTHERN MISSISSIPPI · PI KESSL, JACQUES J. · 2016 to 2017
$406k
NIAID NIH HHS R21 AI127282NIGMS NIH HHS P20 GM103476NIGMS NIH HHS R15 GM129751
6 · The paper itself

Abstract

A convenient two-step synthesis of ethyl 4-hydroxy-2-methylquinoline-3-carboxylate derivatives has been developed starting from commercially available 2-aminobenzoic acids. In step 1, the anthranilic acids are smoothly converted to isatoic anhydrides using solid triphosgene in THF. In step 2, the anhydride electrophiles are reacted with the sodium enolate of ethyl acetoacetate, generated from sodium hydroxide, in warm

Indexed as

cyclodehydrationHIV integraseisatoic anhydridemasked acyl cyanidequinoline

Identifiers

PMID30344776
PMCPMC6178280
OpenAlexW2893629622

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.