Evidence map›Paper›PMID 42462119›Full record

ArticleJournal of the American Chemical Society2026

Photocatalytic Denitrative Homo- and Cross-Coupling of Nitroalkanes toward the Synthesis of Alkenes.

Max Dietel, Mangish Ghosh, Hendrik Paps, Zen Shimizu, Jonas Scholl, Michael Andreas Gruber, Oliver Reiser

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. 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. Photo-Stitching of Nitroalkanes via Cross-Denitrative Olefination.Journal of the American Chemical Society · 2026
    Article
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

7 authors.

Max DietelInstitut für Organische Chemie, Universität Regensburg, Regensburg93053, Germany.ORCID 0009-0000-7592-8995
Mangish GhoshInstitut für Organische Chemie, Universität Regensburg, Regensburg93053, Germany.ORCID 0009-0005-2632-303X
Hendrik PapsInstitut für Organische Chemie, Universität Regensburg, Regensburg93053, Germany.
Zen ShimizuInstitut für Organische Chemie, Universität Regensburg, Regensburg93053, Germany.
Jonas SchollInstitut für Organische Chemie, Universität Regensburg, Regensburg93053, Germany.
Michael Andreas GruberKlinik für Anästhesiologie, Universitätsklinikum Regensburg, Regensburg93053, Germany.
Oliver ReiserInstitut für Organische Chemie, Universität Regensburg, Regensburg93053, Germany.ORCID 0000-0003-1430-573X

Funding

Elitenetzwerk Bayern NAGerman Research Council (DFG) TRR 325444632635-A2
6 · The paper itself

Abstract

Alkenes serve as fundamental motifs across natural products and synthetic molecules, yet efficient, mild, and versatile olefination strategies remain in demand. Nitroalkanes, renowned for their broad reactivity as nucleophiles or corresponding radicals, still offer untapped potential in photocatalysis. Here, we report a unified, photocatalyzed generation of α-nitroalkyl radicals via oxidation of simple, nonprefunctionalized nitronates, followed by addition to another nitronate (formal homo- or cross-coupling) and subsequent double denitration to furnish alkenes. This transformation leverages both the pro-nucleophilic and pro-electrophilic nature of nitroalkanes, challenging the classic McMurry-type coupling protocol. Moreover, the synthetic manifold is scalable and demonstrates its applicability by synthesizing medicinally relevant Combretastatin and lignan-type cores.

Identifiers

PMID42462119
PMCPMC13450380

What OpenQuestion holds

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LicenceCC BY
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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.