Evidence map›Paper›PMID 41716244›Full record

ReviewChemical science2026

Control over stereogenic centres beyond tetracoordination.

Anton Budeev, Christof Sparr

Abstract readReview
In one paragraph

Review in Chemical science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Anton BudeevDepartment of Chemistry, University of Basel St. Johanns-Ring 19 Basel 4056 Switzerland christof.sparr@unibas.ch.ORCID https://orcid.org/0009-0000-3358-0396
Christof SparrDepartment of Chemistry, University of Basel St. Johanns-Ring 19 Basel 4056 Switzerland christof.sparr@unibas.ch.ORCID https://orcid.org/0000-0002-4213-0941

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In contrast to conventional tetracoordinate stereogenic centres exhibiting twofold stereogenicity, penta- and hexacoordinate stereogenic centres may encode more than two stereoisomers, expanding the stereochemical space accessible to these species. This more complex stereoisomerism is characteristic to compounds of a variety of main-group elements and transition metals having a suitable set of ligands. Despite these unique hallmarks and the prospective applications in medicinal chemistry, catalysis, and information science, this area of stereoselective synthesis awaits widespread exploration. In this review, the fundamentals of the higher-order stereogenicity of penta- and hexacoordinate stereogenic centres will thus be summarized and an overview of emerging applications and their stereoselective synthesis will be provided.

Identifiers

PMID41716244
PMCPMC12915501

What OpenQuestion holds

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Registered trials

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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.