Evidence map›Paper›PMID 35517552›Full record

ArticleRSC advances2020

Stereoselective synthesis and application of isopulegol-based bi- and trifunctional chiral compounds.

Tam Minh Le, Thu Huynh, Gábor Endre, András Szekeres, Ferenc Fülöp, Zsolt Szakonyi

Open access · goldAbstract read
In one paragraph

Article in RSC advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Pharmaceuticals (Basel, Switzerland) · 2025
    Article
  3. Article
  4. Monoterpene Hydroxy Lactones Isolated fromMolecules (Basel, Switzerland) · 2024
    Article
  5. Article
  6. Article
  7. Biotransformation of (-)-Isopulegol byPharmaceuticals (Basel, Switzerland) · 2022
    Article
  8. Novel (+)-Neoisopulegol-BasedInternational journal of molecular sciences · 2021
    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 at 1 institution in 1 country.

Tam Minh LeInstitute of Pharmaceutical Chemistry, University of Szeged, Interdisciplinary Excellence Centre Eötvös utca 6 H-6720 Szeged Hungary leminhtam@pharm.u-szeged.hu fulop@pharm.u-szeged.hu szakonyi@pharm.u-szeged.hu +36-62-545705 +36-62-546809.ORCID https://orcid.org/0000-0002-8296-887X
Thu HuynhDepartment of Microbiology, University of Szeged Közép fasor 52 6726 Szeged Hungary huynh_thu@hcmut.edu.vn egabcy@gmail.com andras.j.szekeres@gmail.com.ORCID https://orcid.org/0000-0001-6042-3353
Gábor EndreDepartment of Microbiology, University of Szeged Közép fasor 52 6726 Szeged Hungary huynh_thu@hcmut.edu.vn egabcy@gmail.com andras.j.szekeres@gmail.com.
András SzekeresDepartment of Microbiology, University of Szeged Közép fasor 52 6726 Szeged Hungary huynh_thu@hcmut.edu.vn egabcy@gmail.com andras.j.szekeres@gmail.com.ORCID https://orcid.org/0000-0003-1651-4623
Ferenc FülöpInstitute of Pharmaceutical Chemistry, University of Szeged, Interdisciplinary Excellence Centre Eötvös utca 6 H-6720 Szeged Hungary leminhtam@pharm.u-szeged.hu fulop@pharm.u-szeged.hu szakonyi@pharm.u-szeged.hu +36-62-545705 +36-62-546809.ORCID https://orcid.org/0000-0003-1066-5287
Zsolt SzakonyiInstitute of Pharmaceutical Chemistry, University of Szeged, Interdisciplinary Excellence Centre Eötvös utca 6 H-6720 Szeged Hungary leminhtam@pharm.u-szeged.hu fulop@pharm.u-szeged.hu szakonyi@pharm.u-szeged.hu +36-62-545705 +36-62-546809.ORCID https://orcid.org/0000-0003-2432-8409
University of Szeged · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A new family of isopulegol-based bi- and trifunctional chiral ligands was developed from commercially available (-)-isopulegol. Nucleophilic addition of primary amines towards (+)-α-methylene-γ-butyrolactone was accomplished, followed by reduction of the obtained β-aminolactones to provide aminodiols in highly stereoselective reactions. Epoxidation of (-)-isopulegol and subsequent oxirane ring opening with primary amines resulted in

Identifiers

PMID35517552
PMCPMC9057261
OpenAlexW3093003688

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.