Evidence map›Paper›PMID 37065181›Full record

ArticleACS catalysis2022

Zinc-Free, Scalable Reductive Cross-Electrophile Coupling Driven by Electrochemistry in an Undivided Cell.

Mareena C Franke, Victoria R Longley, Mohammad Rafiee, Shannon S Stahl, Eric C Hansen, Daniel J Weix

Open access · greenAbstract read
In one paragraph

Article in ACS catalysis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
9.4field-weighted citation impact, top 1% 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

27 citing papers in PubMed, 87 citations in OpenAlex.

  1. Article
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  3. Review
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  5. Article
  6. Borohydride Oxidation as Counter Reaction in Reductive Electrosynthesis.Angewandte Chemie (International ed. in English) · 2025
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
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  16. Article
  17. Nickel-Catalyzed Electrochemical Cross-Electrophile C(spAngewandte Chemie (International ed. in English) · 2024
    Article
  18. Article
  19. Article
  20. 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

6 authors at 3 institutions in 1 country.

Mareena C FrankeDepartment of Chemistry, University of Wisconsin-Madison, Madison, WI 53706 USA.
Victoria R LongleyDepartment of Chemistry, University of Wisconsin-Madison, Madison, WI 53706 USA.
Mohammad RafieeDepartment of Chemistry, University of Missouri-Kansas City, Kansas City, MO 64110 USA.
Shannon S StahlDepartment of Chemistry, University of Wisconsin-Madison, Madison, WI 53706 USA.
Eric C HansenChemical Research and Development, Pfizer, Inc., Eastern Point Road, Groton, CT 06340 USA.
Daniel J WeixDepartment of Chemistry, University of Wisconsin-Madison, Madison, WI 53706 USA.
University of Wisconsin–Madison · USPfizer (United States) · USUniversity of Missouri–Kansas City · US

Funding

Reductive Coupling Reactions: Trading Organometallic Reagents for Organic HalidesR01GM097243 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI Daniel John Weix · 2011 to 2026
$5.6M
Catalytic Redox Reactions for Pharmaceutical SynthesisR35GM134929 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI Shannon S Stahl · 2020 to 2026
$4.3M
NIGMS NIH HHS R01 GM097243NIGMS NIH HHS R35 GM134929
6 · The paper itself

Abstract

Nickel-catalyzed reductive cross-electrophile coupling reactions are becoming increasingly important in organic synthesis, but application at scale is limited by three interconnected challenges: a reliance on amide solvents (complicated workup, regulated), the generation of stoichiometric Zn salts (complicated isolation, waste disposal issue), and mixing/activation challenges of zinc powder. We show here an electrochemical approach that addresses these three issues: the reaction works in acetonitrile with diisopropylethylamine as the terminal reductant in a simple undivided cell (graphite(+)/nickel foam(-)). The reaction utilizes a combination of two ligands, 4,4'-di-

Indexed as

cross-couplingcross-electrophile couplingelectrochemistryflowmechanismmultimetallic catalysisnickel

Identifiers

PMID37065181
PMCPMC10101217
OpenAlexW4300865504

What OpenQuestion holds

Textmetadata
LicenceTDM
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.