Evidence map›Paper›PMID 33348842›Full record

ArticleMolecules (Basel, Switzerland)2020

Efficient Synthesis of New Fluorinated β-Amino Acid Enantiomers through Lipase-Catalyzed Hydrolysis.

Sayeh Shahmohammadi, Ferenc Fülöp, Enikő Forró

Abstract read
In one paragraph

Article 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 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. Enzymatic synthesis of fluorinated compounds.Applied microbiology and biotechnology · 2021
    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.

Sayeh ShahmohammadiInstitute of Pharmaceutical Chemistry, University of Szeged, H-6720 Szeged, Hungary.
Ferenc FülöpInstitute of Pharmaceutical Chemistry, University of Szeged, H-6720 Szeged, Hungary.ORCID 0000-0003-1066-5287
Enikő ForróInstitute of Pharmaceutical Chemistry, University of Szeged, H-6720 Szeged, Hungary.

Funding

Hungarian Scientific Research Council OTKA K129049Ministry of National Economy, National Research, Development and Innovation Office GINOP, 2.3.2-15-2016-00014
6 · The paper itself

Abstract

An efficient and novel enzymatic method has been developed for the synthesis of β-fluorophenyl-substituted β-amino acid enantiomers through lipase PSIM (

Indexed as

Amino AcidsBurkholderiaFluorineHalogenationHydrolysisLipaseStereoisomerismAmino AcidsFluorineLipaseenantioselective synthesisfluorinated β-amino acidkinetic resolutionlipase-catalyzed hydrolysis

Identifiers

PMID33348842
PMCPMC7766834

What OpenQuestion holds

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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.