Evidence map›Paper›PMID 36234884›Full record

ArticleMolecules (Basel, Switzerland)2022

Detection and Verification of a Key Intermediate in an Enantioselective Peptide Catalyzed Acylation Reaction.

Matthias Brauser, Tim Heymann, Christina Marie Thiele

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

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 at 1 institution in 1 country.

Matthias BrauserClemens-Schöpf-Institute for Organic Chemistry and Biochemistry, Department of Chemistry, Technical University of Darmstadt, Alarich-Weiss-Straße 4, 64287 Darmstadt, Germany.ORCID 0000-0002-0047-1481
Tim HeymannClemens-Schöpf-Institute for Organic Chemistry and Biochemistry, Department of Chemistry, Technical University of Darmstadt, Alarich-Weiss-Straße 4, 64287 Darmstadt, Germany.
Christina Marie ThieleClemens-Schöpf-Institute for Organic Chemistry and Biochemistry, Department of Chemistry, Technical University of Darmstadt, Alarich-Weiss-Straße 4, 64287 Darmstadt, Germany.ORCID 0000-0001-7876-536X
Technische Universität Darmstadt · DE

Funding

Deutsche Forschungsgemeinschaft TH1115/12-1Dr. Hans Messer Stiftung financial support to C.M.T and M.B.Hessian Ministry of Higher Education, Research, and the Arts financial support to T.H.
6 · The paper itself

Abstract

Until now, the intermediate responsible for the acyl transfer of a highly enantioselective tetrapeptide organocatalyst for the kinetic resolution of trans-cycloalkane-1,2-diols has never been directly observed. It was proposed computationally that a π-methylhistidine moiety is acylated as an intermediate step in the catalytic cycle. In this study we set out to investigate whether we can detect and characterize this key intermediate using NMR-spectroscopy and mass spectrometry. Different mass spectrometric experiments using a nano-ElectroSpray Ionization (ESI) source and tandem MS-techniques allowed the identification of tetrapeptide acylium ions using different acylation reagents. The complexes of

Indexed as

CycloparaffinsMethylhistidinesAcylationAlcoholsCatalysisCyclohexanesPeptidesSpectrometry, Mass, Electrospray IonizationStereoisomerismAlcoholsCyclohexanesCycloparaffinsMethylhistidinesPeptidesacylationimidazolium ionmass spectrometryNMR spectroscopyorganocatalysis

Identifiers

PMID36234884
PMCPMC9571696
OpenAlexW4297546371

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.