Evidence map›Paper›PMID 31052604›Full record

ReviewMolecules (Basel, Switzerland)2019

Al(Salen) Metal Complexes in Stereoselective Catalysis.

Andrea Gualandi, Francesco Calogero, Simone Potenti, Pier Giorgio Cozzi

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2019. 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. Privileged Chiral Photocatalysts.Angewandte Chemie (International ed. in English) · 2025
    Review
  2. Article
  3. Article
  4. Recent Advances in Asymmetric Catalysis Using p-Block Elements.Angewandte Chemie (International ed. in English) · 2024
    Review
  5. Article
  6. Article
  7. Review
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

4 authors.

Andrea GualandiALMA MATER STUDIORUM Università di Bologna, Dipartimento di Chimica "G. Ciamician", Via Selmi 2, 40126 Bologna, Italy. andrea.gualandi10@unibo.it.
Francesco CalogeroALMA MATER STUDIORUM Università di Bologna, Dipartimento di Chimica "G. Ciamician", Via Selmi 2, 40126 Bologna, Italy. francesco.calogero@studio.unibo.it.
Simone PotentiALMA MATER STUDIORUM Università di Bologna, Dipartimento di Chimica "G. Ciamician", Via Selmi 2, 40126 Bologna, Italy. simone.potenti@sns.it.
Pier Giorgio CozziALMA MATER STUDIORUM Università di Bologna, Dipartimento di Chimica "G. Ciamician", Via Selmi 2, 40126 Bologna, Italy. piergiorgio.cozzi@unibo.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Salen ligands are a class of Schiff bases simply obtained through condensation of two molecules of a hydroxyl-substituted aryl aldehyde with an achiral or chiral diamine. The prototype salen, or

Indexed as

CatalysisChemistry Techniques, SyntheticCycloaddition ReactionEthylenediaminesMolecular StructureOrganometallic CompoundsPolymerizationStereoisomerismUridine Diphosphate N-AcetylglucosamineEthylenediaminesOrganometallic Compoundssalen-aluminum complexUDP-N-acetylglucosamine-enolbutyrateUridine Diphosphate N-Acetylglucosaminealuminumaluminum metal complexesbifunctional catalysiscatalysischiral ligandLewis Acidorganic synthesissalenstereoselective reactions

Identifiers

PMID31052604
PMCPMC6540592

What OpenQuestion holds

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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.