Evidence map›Paper›PMID 34641579›Full record

ArticleMolecules (Basel, Switzerland)2021

New Methods for the Synthesis of Spirocyclic Cephalosporin Analogues.

Alan X Zhao, Louise E Horsfall, Alison N Hulme

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. New Synthetic Methodology for Drug-like Molecules.Molecules (Basel, Switzerland) · 2023
    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

3 authors.

Alan X ZhaoEaStChem School of Chemistry, The University of Edinburgh, Joseph Black Building, David Brewster Road, Edinburgh EH9 3FJ, UK.
Louise E HorsfallInstitute of Quantitative Biology, Biochemistry, and Biotechnology, School of Biological Science, The University of Edinburgh, Roger Land Building, Alexander Crum Brown Road, Edinburgh EH9 3FF, UK.ORCID 0000-0003-1594-2992
Alison N HulmeEaStChem School of Chemistry, The University of Edinburgh, Joseph Black Building, David Brewster Road, Edinburgh EH9 3FJ, UK.ORCID 0000-0002-4619-1506

Funding

Engineering and Physical Sciences Research Council EP/M506515/1 and EP/N509644/1Highlands and Islands Enterprise IBioIC (Innovation Centre Programme)Scottish Enterprise IBioIC (Innovation Centre Programme)Scottish Funding Council IBioIC (Innovation Centre Programme)
6 · The paper itself

Abstract

Spiro compounds provide attractive targets in drug discovery due to their inherent three-dimensional structures, which enhance protein interactions, aid solubility and facilitate molecular modelling. However, synthetic methodology for the spiro-functionalisation of important classes of penicillin and cephalosporin β-lactam antibiotics is comparatively limited. We report a novel method for the generation of spiro-cephalosporin compounds through a Michael-type addition to the dihydrothiazine ring. Coupling of a range of catechols is achieved under mildly basic conditions (K

Indexed as

CatecholsCephalosporinsMolecular StructurePenicillinsSpiro CompoundsCatecholsCephalosporinsPenicillinsSpiro CompoundsMichael-type reactionspiro-cephalosporinspiro-cyclisation

Identifiers

PMID34641579
PMCPMC8512572

What OpenQuestion holds

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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.