Evidence map›Paper›PMID 42044481›Full record

ArticleJournal of the American Chemical Society2026

Alkyl Radical Coupling with Phenoxy(imine)-Nickel(II)-Aryl Complexes: Evidence for a Multistep Process in C-C Bond Formation.

Hao Liang, L Reginald Mills, Marina Perez-Jimenez, Matthew V Joannou, Heejun Lee, Steven R Wisniewski, Eric M Simmons, Karla Ravin, Paul J Chirik

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. 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

9 authors.

Hao LiangDepartment of Chemistry, Princeton University, Princeton, New Jersey 08544, United States.
L Reginald MillsDepartment of Chemistry, Princeton University, Princeton, New Jersey 08544, United States.ORCID 0000-0002-6329-2368
Marina Perez-JimenezDepartment of Chemistry, Princeton University, Princeton, New Jersey 08544, United States.ORCID 0000-0001-7891-4273
Matthew V JoannouChemical Process Development, Bristol Myers Squibb Company, New Brunswick, New Jersey 08903, United States.ORCID 0000-0002-0079-7107
Heejun LeeChemical Process Development, Bristol Myers Squibb Company, New Brunswick, New Jersey 08903, United States.ORCID 0000-0002-0439-3863
Steven R WisniewskiChemical Process Development, Bristol Myers Squibb Company, New Brunswick, New Jersey 08903, United States.ORCID 0000-0001-6035-4394
Eric M SimmonsChemical Process Development, Bristol Myers Squibb Company, New Brunswick, New Jersey 08903, United States.ORCID 0000-0002-3854-1561
Karla RavinDepartment of Chemistry, Princeton University, Princeton, New Jersey 08544, United States.
Paul J ChirikDepartment of Chemistry, Princeton University, Princeton, New Jersey 08544, United States.ORCID 0000-0001-8473-2898

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The reaction of well-defined phenoxy(imine)-nickel(II)-aryl complexes with alkyl radicals was investigated en route to C-C bond formation. A 4-dimethylaminopyridine-titanium tris(anilide) complex was identified as a selective reagent for halogen-atom abstraction of unactivated alkyl halides, generating alkyl radicals that were subsequently captured by phenoxy(imine)-nickel(II)-aryl complexes. A combination of radical clock and competition experiments provided insight into ligand effects on both the phenoxy(imine) and the nickel-aryl in radical capture and subsequent C-C bond formation. Differences between parallel and competition radical clock experiments support a multistep process for C-C bond formation. Results from

Identifiers

PMID42044481
PMCPMC13154193

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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.