Evidence map›Paper›PMID 41556390›Full record

ArticleJournal of the American Chemical Society2026

Iridium-Catalyzed Stereoselective α-Alkylation of α-Hydroxy Ketones with Minimally Polarized Alkenes.

Yihong Wang, Fenglin Hong, Craig M Robertson, Richard J Mudd, John F Bower

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 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

5 authors.

Yihong WangDepartment of Chemistry, University of Liverpool, Crown Street, Liverpool L69 7ZD, United Kingdom.
Fenglin HongDepartment of Chemistry, University of Liverpool, Crown Street, Liverpool L69 7ZD, United Kingdom.
Craig M RobertsonDepartment of Chemistry, University of Liverpool, Crown Street, Liverpool L69 7ZD, United Kingdom.
Richard J MuddDepartment of Chemistry, University of Liverpool, Crown Street, Liverpool L69 7ZD, United Kingdom.
John F BowerDepartment of Chemistry, University of Liverpool, Crown Street, Liverpool L69 7ZD, United Kingdom.ORCID 0000-0002-7551-8221

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cationic Ir(I)-complexes modified with homochiral diphosphines promote the α-C-H addition of α-hydroxy ketones to styrenes or alkyl olefins. These processes are predicated on the hydroxyl-directed formation of an Ir-enolate. Inter- and intramolecular processes are feasible, with the latter offering stereocontrolled access to carbocycles bearing two new stereocenters. The intramolecular processes constitute rare examples of alkene-based Conia-ene reactions that are enantio- and diastereoselective.

Identifiers

PMID41556390
PMCPMC12879937

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.