Evidence map›Paper›PMID 34964164›Full record

ArticleChirality2022

Enantioselective synthesis and selective functionalization of 4-aminotetrahydroquinolines as novel GLP-1 secretagogues.

Mustafa Z Kazancioglu, Kevin Quirion, Peter Wipf, Erin M Skoda

Abstract read
In one paragraph

Article in Chirality, 2022. 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

4 authors.

Mustafa Z KazanciogluDepartment of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.ORCID 0000-0001-5189-2051
Kevin QuirionDepartment of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Peter WipfDepartment of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.ORCID 0000-0001-7693-5863
Erin M SkodaDepartment of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Funding

University of Pittsburgh Center for Chemical DiversityP50GM067082 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WIPF, PETER · 2002 to 2012
$18.6M
NIGMS NIH HHS P50 GM067082NIH HHS 2P50GM067082NIH HHS DOD Award W81XWH-18-1-0623
6 · The paper itself

Abstract

Polysubstituted tetrahydroquinolines were obtained in moderate to high yields (28% to 92%) and enantiomeric ratios (er 89:11 to 99:1) by a three-component Povarov reaction using a chiral phosphoric acid catalyst. Significantly, post-Povarov functional group interconversions allowed a rapid access to a library of 36 enantioenriched 4-aminotetrahydroquinoline derivatives featuring five points of diversity. Selected analogs were assayed for their ability to function as glucagon-like peptide-1 (GLP-1) secretagogues.

Indexed as

Glucagon-Like Peptide 1SecretagoguesCatalysisStereoisomerismGlucagon-Like Peptide 1Secretagogues4-aminotetrahydroquinolineasymmetric catalysischiral phosphoric aciddiversity-oriented synthesisGLP-1 secretagoguesPovarov reaction

Identifiers

PMID34964164
PMCPMC8837726

What OpenQuestion holds

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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.