Evidence map›Paper›PMID 35910461›Full record

ArticleEuropean journal of organic chemistry2022

A Modular Synthesis of Teraryl-Based α-Helix Mimetics, Part 5: A Complete Set of Pyridine Boronic Acid Pinacol Esters Featuring Side Chains of Proteinogenic Amino Acids.

Melanie Trobe, Till Schreiner, Martin Vareka, Sebastian Grimm, Bernhard Wölfl, Rolf Breinbauer

Abstract read
In one paragraph

Article in European journal of organic chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Enantioselective Total Synthesis of Two Aromatized Halicyclamines.Journal of the American Chemical Society · 2026
    Article
  2. Article
  3. Aromatic oligoesters as novel helix mimetic scaffolds.Bioorganic & medicinal chemistry · 2023
    Article
  4. Article
  5. Article
  6. 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

6 authors.

Melanie TrobeInstitute of Organic Chemistry Graz University of Technology Stremayrgasse 9 8010 Graz Austria.
Till SchreinerInstitute of Organic Chemistry Graz University of Technology Stremayrgasse 9 8010 Graz Austria.
Martin VarekaInstitute of Organic Chemistry Graz University of Technology Stremayrgasse 9 8010 Graz Austria.
Sebastian GrimmInstitute of Organic Chemistry Graz University of Technology Stremayrgasse 9 8010 Graz Austria.
Bernhard WölflInstitute of Organic Chemistry Graz University of Technology Stremayrgasse 9 8010 Graz Austria.
Rolf BreinbauerInstitute of Organic Chemistry Graz University of Technology Stremayrgasse 9 8010 Graz Austria.ORCID 0000-0001-6009-7359

Funding

Austrian Science Fund FWF I 2712
6 · The paper itself

Abstract

Teraryl-based α-helix mimetics have proven to be useful compounds for the inhibition of protein-protein interactions (PPI). We have developed a modular and flexible approach for the synthesis of teraryl-based α-helix mimetics using pyridine containing boronic acid building blocks to increase the water solubility. Following our initial publication in which we have introduced the methodology in combination with sequential Pd-catalyzed cross-coupling for teraryl assembly, we can now report a complete set of pyridine based boronic acid building blocks decorated with side chains of all proteinogenic amino acids relevant for PPI (Ala, Arg, Asn, Asp, Cys, Gln, Glu, His, Ile, Leu, Lys, Met, Phe, Ser, Thr, Trp, Tyr, Val) to complement the core fragment set. For a representative set of teraryls we have studied the influence of the pyridine rings on the solubility of the assembled oligoarenes.

Indexed as

BorylationCross-couplingPeptide mimeticsProtein-protein interactionsPyridine boronic acid pinacol ester

Identifiers

PMID35910461
PMCPMC9304165

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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.