Evidence map›Paper›PMID 35096179›Full record

ArticleBeilstein journal of organic chemistry2022

Regioselective synthesis of methyl 5-(

Jolita Bruzgulienė, Greta Račkauskienė, Aurimas Bieliauskas, Vaida Milišiūnaitė, Miglė Dagilienė, Gita Matulevičiūtė, Vytas Martynaitis, Sonata Krikštolaitytė, Frank A Sløk, Algirdas Šačkus

Abstract read
In one paragraph

Article in Beilstein 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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Facile synthesis of newRSC advances · 2023
    Article
  6. Article
  7. 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

10 authors.

Jolita BruzgulienėInstitute of Synthetic Chemistry, Kaunas University of Technology, K. Baršausko g. 59, Kaunas LT-51423, Lithuania.
Greta RačkauskienėInstitute of Synthetic Chemistry, Kaunas University of Technology, K. Baršausko g. 59, Kaunas LT-51423, Lithuania.
Aurimas BieliauskasInstitute of Synthetic Chemistry, Kaunas University of Technology, K. Baršausko g. 59, Kaunas LT-51423, Lithuania.ORCID https://orcid.org/0000-0002-3838-261X
Vaida MilišiūnaitėInstitute of Synthetic Chemistry, Kaunas University of Technology, K. Baršausko g. 59, Kaunas LT-51423, Lithuania.ORCID https://orcid.org/0000-0002-5338-4621
Miglė DagilienėInstitute of Synthetic Chemistry, Kaunas University of Technology, K. Baršausko g. 59, Kaunas LT-51423, Lithuania.
Gita MatulevičiūtėInstitute of Synthetic Chemistry, Kaunas University of Technology, K. Baršausko g. 59, Kaunas LT-51423, Lithuania.
Vytas MartynaitisDepartment of Organic Chemistry, Kaunas University of Technology, Radvilėnų pl. 19, Kaunas LT-50254, Lithuania.ORCID https://orcid.org/0000-0003-1147-6584
Sonata KrikštolaitytėDepartment of Organic Chemistry, Kaunas University of Technology, Radvilėnų pl. 19, Kaunas LT-50254, Lithuania.
Frank A SløkVipergen ApS, Gammel Kongevej 23A, DK-1610 Copenhagen V, Denmark.
Algirdas ŠačkusInstitute of Synthetic Chemistry, Kaunas University of Technology, K. Baršausko g. 59, Kaunas LT-51423, Lithuania.ORCID https://orcid.org/0000-0002-1514-4934

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A convenient and efficient synthesis of novel achiral and chiral heterocyclic amino acid-like building blocks was developed. Regioisomeric methyl 5-(

Indexed as

1,2-oxazole (isoxazole)13C15N)15N-labeled 1,2-oxazoleheterocyclic amino acidsNMR (1HX-ray structure analysisβ-enamino ketoesters

Identifiers

PMID35096179
PMCPMC8767561

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.