Evidence map›Paper›PMID 41150968›Full record

ArticleJournal of the American Chemical Society2025

One-Electron Approach for Trans-Selective Alkyne Semi-Reduction via Cobalt Catalysis.

Rakesh Mondal, Lior Galmidi, Avra Tzaguy, Tal Sason, Moran Feller, Mark A Iron, Liat Avram, Ronny Neumann, Samer Gnaim

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Electrochemical Hydrogenation of Aza-Arenes Using HJournal of the American Chemical Society · 2026
    Article
  2. 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

9 authors.

Rakesh MondalDepartment of Molecular Chemistry and Materials Science, Weizmann Institute of Science, Rehovot 7610001, Israel.
Lior GalmidiDepartment of Molecular Chemistry and Materials Science, Weizmann Institute of Science, Rehovot 7610001, Israel.
Avra TzaguyDepartment of Molecular Chemistry and Materials Science, Weizmann Institute of Science, Rehovot 7610001, Israel.ORCID 0000-0003-3647-7882
Tal SasonDepartment of Molecular Chemistry and Materials Science, Weizmann Institute of Science, Rehovot 7610001, Israel.
Moran FellerDepartment of Molecular Chemistry and Materials Science, Weizmann Institute of Science, Rehovot 7610001, Israel.ORCID 0000-0001-7436-9183
Mark A IronDepartment of Chemical Research Support, Weizmann Institute of Science, Rehovot 7610001, Israel.ORCID 0000-0001-9774-2358
Liat AvramDepartment of Chemical Research Support, Weizmann Institute of Science, Rehovot 7610001, Israel.ORCID 0000-0001-6535-3470
Ronny NeumannDepartment of Molecular Chemistry and Materials Science, Weizmann Institute of Science, Rehovot 7610001, Israel.ORCID 0000-0002-5530-1287
Samer GnaimDepartment of Molecular Chemistry and Materials Science, Weizmann Institute of Science, Rehovot 7610001, Israel.ORCID 0000-0001-9030-4195

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The diastereoselective semireduction of alkynes to alkenes is a powerful transformation in synthetic chemistry, yet catalytic methods for trans-selective (E) alkyne reduction remain limited. Herein, we introduce a fundamentally new approach for the highly selective trans-semireduction of internal alkynes, enabled by a cobalt-catalyzed electrochemical radical pathway. This method offers a broad substrate scope, accommodating alkynes with diverse electronic and steric profiles, and displays exceptional chemoselectivity and functional group tolerance. The methodology was extended to isotopically labeled trans-deuteration and demonstrated excellent chemoselectivity in substrates containing multiple alkyne motifs. Mechanistic studies, including cyclic voltammetry, UV-vis spectroelectrochemistry, and DFT calculations, support a dual catalytic cycle involving electrochemical Co-H formation and a subsequent organometallic radical pathway. Insights from this mechanism guided the development of a complementary chemical oxidative protocol, enabling access to

Identifiers

PMID41150968
PMCPMC12616701

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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.