Evidence map›Paper›PMID 41533487›Full record

ArticleChemistry, an Asian journal2026

Copper-Catalyzed Asymmetric Hydroboration of Cyclic Dienes.

Jieun You, Jung Tae Han, Jaesook Yun

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Chemistry, an Asian journal, 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
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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

3 authors.

Jieun YouDepartment of Chemistry, Sungkyunkwan University, Suwon, South Korea.
Jung Tae HanChemical and Biological Integrative Research Center, Korea Institute of Science and Technology, Seoul, South Korea.
Jaesook YunDepartment of Chemistry, Sungkyunkwan University, Suwon, South Korea.ORCID https://orcid.org/0000-0003-4380-7878

Funding

Korea Basic Science Institute (National research Facilities and Equipment Center) RS-2022-NF000854Korea Basic Science Institute (National research Facilities and Equipment Center) RS-2022-NF001081National Research Foundation of Korea RS-2023-00219859National Research Foundation of Korea RS-2025-00518845Samsung Science and Technology Foundation SSTF-BA2002-08
6 · The paper itself

Abstract

A copper-catalyzed enantioselective hydroboration of cyclic dienes, which afford enantioenriched allylboronates, is disclosed. This reaction is catalyzed by a chiral bisphosphine-Cu complex in combination with commercially available pinacolborane as the hydroborane source. The method is applicable to 1-aryl-cyclohexadienes and 1,2-dihydropyridine derivatives, affording allylboronate products in high regio- and enantioselectivity. The obtained allylboronates serve as versatile intermediates for the synthesis of diverse chiral compounds.

Indexed as

coppercyclic dienesenantioselectivityhydroborationregioselectivity

Identifiers

PMID41533487
PMCPMC13394298

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.