Evidence map›Paper›PMID 37441237›Full record

ArticleACS catalysis2023

Insight into Radical Initiation, Solvent Effects, and Biphenyl Production in Iron-Bisphosphine Cross-Couplings.

Maria Camila Aguilera, Achyut Ranjan Gogoi, Wes Lee, Lei Liu, William W Brennessel, Osvaldo Gutierrez, Michael L Neidig

Open access · hybridAbstract read
In one paragraph

Article in ACS catalysis, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.9field-weighted citation impact, top 6% of its field
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

12 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Iron-mediated C(spTetrahedron · 2025
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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 at 4 institutions in 2 countries.

Maria Camila AguileraDepartment of Chemistry, University of Rochester, Rochester, New York 14627, United States.
Achyut Ranjan GogoiDepartment of Chemistry, Texas A&M University, College Station, Texas 77843, United States.ORCID https://orcid.org/0000-0002-7609-3720
Wes LeeDepartment of Chemistry and Biochemistry, University of Maryland, College Park, Maryland 20742, United States.
Lei LiuDepartment of Chemistry, Texas A&M University, College Station, Texas 77843, United States.ORCID https://orcid.org/0000-0002-1708-9246
William W BrennesselDepartment of Chemistry, University of Rochester, Rochester, New York 14627, United States.ORCID https://orcid.org/0000-0001-5461-1825
Osvaldo GutierrezDepartment of Chemistry, Texas A&M University, College Station, Texas 77843, United States.ORCID https://orcid.org/0000-0001-8151-7519
Michael L NeidigDepartment of Chemistry, University of Rochester, Rochester, New York 14627, United States.ORCID https://orcid.org/0000-0002-2300-3867
Texas A&M University · USUniversity of Maryland, College Park · USUniversity of Rochester · USUniversity of Oxford · GB

Funding

Iron-Catalyzed Cross-CouplingR01GM111480 · NIGMS · UNIVERSITY OF ROCHESTER · PI NEIDIG, MICHAEL L · 2014 to 2022
$3.1M
New Directions in Sustainable Open-Shell Radical C-C Bond Formations Enabled by Merging Modern Computational and Experimental MethodsR35GM137797 · NIGMS · UNIV OF MARYLAND, COLLEGE PARK · PI Osvaldo Gutierrez · 2020 to 2026
$2.7M
NIGMS NIH HHS R01 GM111480NIGMS NIH HHS R35 GM137797
6 · The paper itself

Abstract

Iron-bisphosphines have attracted broad interest as highly effective and versatile catalytic systems for two- and three-component cross-coupling strategies. While recent mechanistic studies have defined the role of organoiron(II)-bisphosphine species as key intermediates for selective cross-coupled product formation in these systems, mechanistic features that are essential for catalytic performance remain undefined. Specifically, key questions include the following: what is the generality of iron(II) intermediates for radical initiation in cross-couplings? What factors control reactivity toward homocoupled biaryl side-products in these systems? Finally, what are the solvent effects in these reactions that enable high catalytic performance? Herein, we address these key questions by examining the mechanism of enantioselective coupling between α-chloro- and α-bromoalkanoates and aryl Grignard reagents catalyzed by chiral bisphosphine-iron complexes. By employing freeze-trapped

Identifiers

PMID37441237
PMCPMC10334425
OpenAlexW4381804070

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.