Evidence map›Paper›PMID 40758416›Full record

ArticleOrganic letters2025

Light-Mediated Binaphthyl Enhanced [2 + 2] Dearomatization of Heterocycles via an Energy-Transfer Process.

Maurizio Chiminelli, Carlotta Galbardi, Raimondo Maggi, Franca Bigi, Luca Capaldo, Nicola Della Ca', Rosanna Viscardi, Luciano Marchiò, Giovanni Maestri, Matteo Lanzi

Abstract read
In one paragraph

Article in Organic letters, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Visible-Light Mediated Activation of 1,3-Dienes and Allenes via Energy Transfers.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025
    Review
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.

Maurizio ChiminelliDepartment of Chemistry, Life Sciences and Environmental Sustainability, Università di Parma, Parco Area delle Scienze, 17/A, 43124 Parma, Italy.
Carlotta GalbardiDepartment of Chemistry, Life Sciences and Environmental Sustainability, Università di Parma, Parco Area delle Scienze, 17/A, 43124 Parma, Italy.
Raimondo MaggiDepartment of Chemistry, Life Sciences and Environmental Sustainability, Università di Parma, Parco Area delle Scienze, 17/A, 43124 Parma, Italy.ORCID 0000-0003-3811-7186
Franca BigiDepartment of Chemistry, Life Sciences and Environmental Sustainability, Università di Parma, Parco Area delle Scienze, 17/A, 43124 Parma, Italy.
Luca CapaldoDepartment of Chemistry, Life Sciences and Environmental Sustainability, Università di Parma, Parco Area delle Scienze, 17/A, 43124 Parma, Italy.ORCID 0000-0001-7114-267X
Nicola Della Ca'Department of Chemistry, Life Sciences and Environmental Sustainability, Università di Parma, Parco Area delle Scienze, 17/A, 43124 Parma, Italy.ORCID 0000-0002-7853-7954
Rosanna ViscardiENEA, Casaccia Research Center, 00123 Santa Maria di Galeria, Rome, Italy.ORCID 0000-0001-7861-0288
Luciano MarchiòDepartment of Chemistry, Life Sciences and Environmental Sustainability, Università di Parma, Parco Area delle Scienze, 17/A, 43124 Parma, Italy.ORCID 0000-0002-0025-1104
Giovanni MaestriDepartment of Chemistry, Life Sciences and Environmental Sustainability, Università di Parma, Parco Area delle Scienze, 17/A, 43124 Parma, Italy.ORCID 0000-0002-0244-8605
Matteo LanziDepartment of Chemistry, Life Sciences and Environmental Sustainability, Università di Parma, Parco Area delle Scienze, 17/A, 43124 Parma, Italy.ORCID 0000-0003-0254-7977

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Three-dimensional heterocycles are crucial in medicinal chemistry, yet efficient methods for their preparation remain limited. We report a light-mediated [2 + 2] dearomatization strategy for simple and benzo-fused heteroaromatics via energy-transfer activation. A binaphthyl cocatalyst combined with an Ir-photocatalyst enables high yields and selectivity under mild conditions. Mechanistic studies reveal the fundamental role of the cocatalyst in stabilizing reactive intermediates via dispersion interactions. The versatility of the products was demonstrated through synthetic applications that smoothly increased the molecular complexity.

Identifiers

PMID40758416
PMCPMC12362593

What OpenQuestion holds

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Registered trials

None linked

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.