Evidence map›Paper›PMID 32485034›Full record

ArticleAngewandte Chemie (International ed. in English)2020

Triarylborane-Catalyzed Alkenylation Reactions of Aryl Esters with Diazo Compounds.

Ayan Dasgupta, Katarína Stefkova, Rasool Babaahmadi, Lukas Gierlichs, Alireza Ariafard, Rebecca L Melen

Erratum issuedAbstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. B(COrganic letters · 2023
    Article
  4. B(CRSC advances · 2022
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Site-Selective CJournal of the American Chemical Society · 2021
    Article
  10. Article
  11. Triarylborane-Catalyzed Alkenylation Reactions of Aryl Esters with Diazo Compounds.Angewandte Chemie (International ed. in English) · 2020
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Ayan DasguptaCardiff Catalysis Institute, School of Chemistry, Cardiff University, Main Building, Park Place, Cardiff, CF10 3AT, Cymru/Wales, UK.ORCID http://orcid.org/0000-0001-9945-8334
Katarína StefkovaCardiff Catalysis Institute, School of Chemistry, Cardiff University, Main Building, Park Place, Cardiff, CF10 3AT, Cymru/Wales, UK.ORCID http://orcid.org/0000-0002-5250-0678
Rasool BabaahmadiSchool of Natural Sciences - Chemistry, University of Tasmania, Private Bag 75, Hobart, Tasmania, 7001, Australia.ORCID http://orcid.org/0000-0002-2580-6217
Lukas GierlichsCardiff Catalysis Institute, School of Chemistry, Cardiff University, Main Building, Park Place, Cardiff, CF10 3AT, Cymru/Wales, UK.ORCID http://orcid.org/0000-0002-7815-4697
Alireza AriafardSchool of Natural Sciences - Chemistry, University of Tasmania, Private Bag 75, Hobart, Tasmania, 7001, Australia.ORCID http://orcid.org/0000-0003-2383-6380
Rebecca L MelenCardiff Catalysis Institute, School of Chemistry, Cardiff University, Main Building, Park Place, Cardiff, CF10 3AT, Cymru/Wales, UK.ORCID http://orcid.org/0000-0003-3142-2831

Funding

Engineering and Physical Sciences Research Council EP/R026912/1
6 · The paper itself

Abstract

Herein we report a facile, mild reaction protocol to form carbon-carbon bonds in the absence of transition metal catalysts. We demonstrate the metal-free alkenylation reactions of aryl esters with α-diazoesters to give highly functionalized enyne products. Catalytic amounts of tris(pentafluorophenyl)borane (10-20 mol %) are employed to afford the C=C coupled products (31 examples) in good to excellent yields (36-87 %). DFT studies were used to elucidate the mechanism for this alkenylation reaction.

Indexed as

alkenylationdiazoestersmetal-free catalysistris(pentafluorophenyl)borane

Identifiers

PMID32485034
PMCPMC7497215

What OpenQuestion holds

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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.