Evidence map›Paper›PMID 41726724›Full record

ArticleACS omega2026

Catalyst-Controlled Regio- and Enantioselective Hydrophosphination of α,β-Unsaturated Pyridyl Ketones.

Wendi Shao, Xiufei Nong, Guiyong Wang, Jiuling Li, Baomin Fan, Yafei Guo

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in ACS omega, 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

6 authors.

Wendi ShaoSchool of Chemistry & Environment, Yunnan Minzu University, 2929 Yuehua Road, Kunming 650500, China.
Xiufei NongSchool of Chemistry & Environment, Yunnan Minzu University, 2929 Yuehua Road, Kunming 650500, China.
Guiyong WangSchool of Chemistry & Environment, Yunnan Minzu University, 2929 Yuehua Road, Kunming 650500, China.
Jiuling LiSchool of Chemistry & Environment, Yunnan Minzu University, 2929 Yuehua Road, Kunming 650500, China.
Baomin FanSchool of Chemistry & Environment, Yunnan Minzu University, 2929 Yuehua Road, Kunming 650500, China.
Yafei GuoSchool of Chemistry & Environment, Yunnan Minzu University, 2929 Yuehua Road, Kunming 650500, China.ORCID https://orcid.org/0000-0001-8720-3887

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Here, we present an enantioselective and regioselective hydrophosphination of α,β-unsaturated substrates that feature both ketone and pyridine bifunctional groups. Interestingly, the activation of pyridine and ketone functionalities is selectively achieved through chiral phosphoric acid and oxazaborolidine, respectively. The regioselectivity of the phosphine nucleophiles toward the products can be well controlled by the choice of catalysts. In addition, the α-chiral phosphorus-containing pyridine products exhibit potential applications as chiral

Identifiers

PMID41726724
PMCPMC12917634

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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.