Evidence map›Paper›PMID 40895729›Full record

ArticleRSC advances2025

Cu/Pd dual catalyzed stereoselective construction of vicinal tri- and tetrasubstituted stereocenters connected to chiral α-arylacetonitriles.

Liliane Mimoun, Hamdi Sanaa, Florian Heppner, Hélène Gérard, Laurine Réset, Caroline West, Nicolas Vanthuyne, Pascal Retailleau, Cyril Nicolas, Isabelle Gillaizeau

Abstract read
In one paragraph

Article in RSC advances, 2025. 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

10 authors.

Liliane MimounUniversité d'Orléans, CNRS, UMR 7311, ICOA 45067 Orléans France isabelle.gillaizeau@univ-orleans.fr.
Hamdi SanaaUniversité d'Orléans, CNRS, UMR 7311, ICOA 45067 Orléans France isabelle.gillaizeau@univ-orleans.fr.
Florian HeppnerSorbonne Université, CNRS, Laboratoire de Chimie Théorique, LCT 75005 Paris France.
Hélène GérardSorbonne Université, CNRS, Laboratoire de Chimie Théorique, LCT 75005 Paris France.
Laurine RésetUniversité d'Orléans, CNRS, UMR 7311, ICOA 45067 Orléans France isabelle.gillaizeau@univ-orleans.fr.ORCID https://orcid.org/0009-0008-3737-8468
Caroline WestUniversité d'Orléans, CNRS, UMR 7311, ICOA 45067 Orléans France isabelle.gillaizeau@univ-orleans.fr.ORCID https://orcid.org/0000-0001-7595-6777
Nicolas VanthuyneAix Marseille Univ, CNRS, Central Med, FSCM Marseille France.ORCID https://orcid.org/0000-0003-2598-7940
Pascal RetailleauInstitut de Chimie des Substances Naturelles, UPR 2301, CNRS Gif-sur-Yvette France.
Cyril NicolasUniversité d'Orléans, CNRS, UMR 7311, ICOA 45067 Orléans France isabelle.gillaizeau@univ-orleans.fr.ORCID https://orcid.org/0000-0002-3748-2205
Isabelle GillaizeauUniversité d'Orléans, CNRS, UMR 7311, ICOA 45067 Orléans France isabelle.gillaizeau@univ-orleans.fr.ORCID https://orcid.org/0000-0002-7726-3592

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Herein, we report an optimized Pd/Cu bimetallic catalyst that facilitates the stereoselective allylic alkylation of secondary and tertiary nitriles under mild conditions. This method affords homoallylic nitriles with adjacent tri- and tetrasubstituted stereocenters. Using both racemic and enantioselective catalysts, the system exhibits high regio- and enantioselectivity (ee up to 91%). Mechanistic studies and DFT calculations highlight the key synergistic roles of Pd and Cu in controlling both reactivity and enantioselectivity.

Identifiers

PMID40895729
PMCPMC12395546

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LicenceCC BY-NC
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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.