Evidence map›Paper›PMID 42565650›Full record

ArticleAngewandte Chemie (International ed. in English)2026

Photochemical Reaction Discovery Enabled by the Dynamic Speciation of Copper Complexes.

Alessio Regni, Siyu Liang, Supreeta Sen, Hailey Hendricks, Xijue Wu, Matthew V Pecoraro, Jose B Roque

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 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

7 authors.

Alessio RegniDepartment of Chemistry, Princeton University, Princeton, New Jersey, USA.ORCID https://orcid.org/0000-0002-2188-1789
Siyu LiangDepartment of Chemistry, Princeton University, Princeton, New Jersey, USA.ORCID https://orcid.org/0009-0000-6751-2113
Supreeta SenDepartment of Chemistry, Princeton University, Princeton, New Jersey, USA.ORCID https://orcid.org/0009-0006-4197-281X
Hailey HendricksDepartment of Chemistry, Princeton University, Princeton, New Jersey, USA.ORCID https://orcid.org/0009-0009-3648-8769
Xijue WuDepartment of Chemistry, Princeton University, Princeton, New Jersey, USA.ORCID https://orcid.org/0000-0002-7840-2814
Matthew V PecoraroDepartment of Chemistry, Princeton University, Princeton, New Jersey, USA.ORCID https://orcid.org/0000-0003-2583-5314
Jose B RoqueDepartment of Chemistry, Princeton University, Princeton, New Jersey, USA.ORCID https://orcid.org/0000-0002-5449-1584

Funding

Gordon and Betty Moore FoundationNational Science Foundation Graduate Research FellowshipPrinceton University First-year Graduate FellowshipPrinceton University Start-up Funds
6 · The paper itself

Abstract

Rapid access to molecules with tailored function is essential to advancing the discovery of new medicines, materials, and agrochemicals. Chemical reaction discovery enables it by expanding access to underexplored chemical space and providing more strategies for constructing molecular targets. Among new technologies, photochemical transformations have been revived as a valuable platform for uncovering new reactivity, especially when combined with accelerated reaction discovery platforms. Herein, we report a strategy for accelerated photochemical reaction discovery based on the dynamic speciation of copper complexes, enabled by their metal-ligand bond lability. This approach simplifies reaction screening by employing an earth-abundant copper(II) salt and commercially available ligands to reversibly generate multiple catalytic species in situ, thereby obviating the need for well-defined complexes or photocatalysts. The workflow engaged ubiquitous functional groups in multiple transformations. Specifically, amines and carboxylic acids were employed in deaminative and decarboxylative alkyl azidation of alkenes, enabling the modification of amino acids, peptides, and complex molecules. These products can be further derivatized in one pot through click reactions or by a modular heteroannulation strategy.

Indexed as

catalysiscopperphotoredoxscreeningthree‐component

Identifiers

PMID42565650
PMCPMC13638121

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.