Evidence map›Paper›PMID 32052900›Full record

ArticleAngewandte Chemie (International ed. in English)2020

Tailored Palladium Catalysts for Selective Synthesis of Conjugated Enynes by Monocarbonylation of 1,3-Diynes.

Jiawang Liu, Ji Yang, Carolin Schneider, Robert Franke, Ralf Jackstell, Matthias Beller

Abstract 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. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Pd-Catalyzed Heteroannulation UsingJournal of the American Chemical Society · 2022
    Article
  4. Article
  5. Article
  6. A General and Highly Selective Palladium-Catalyzed Hydroamidation of 1,3-Diynes.Angewandte Chemie (International ed. in English) · 2021
    Article
  7. Article
  8. 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.

Jiawang LiuLeibniz-Institut für Katalyse, Albert-Einstein-Straße 29a, 18059, Rostock, Germany.ORCID http://orcid.org/0000-0002-8548-6286
Ji YangLeibniz-Institut für Katalyse, Albert-Einstein-Straße 29a, 18059, Rostock, Germany.
Carolin SchneiderLeibniz-Institut für Katalyse, Albert-Einstein-Straße 29a, 18059, Rostock, Germany.
Robert FrankeEvonik Performance Materials GmbH, Paul-Baumann-Str. 1, 45772, Marl, Germany.
Ralf JackstellLeibniz-Institut für Katalyse, Albert-Einstein-Straße 29a, 18059, Rostock, Germany.
Matthias BellerLeibniz-Institut für Katalyse, Albert-Einstein-Straße 29a, 18059, Rostock, Germany.ORCID http://orcid.org/0000-0001-5709-0965

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

For the first time, the monoalkoxycarbonylation of easily available 1,3-diynes to give synthetically useful conjugated enynes has been realized. Key to success was the design and utilization of the new ligand 2,2'-bis(tert-butyl(pyridin-2-yl)phosphanyl)-1,1'-binaphthalene (Neolephos), which permits the palladium-catalyzed selective carbonylation under mild conditions, providing a general preparation of functionalized 1,3-enynes in good-to-high yields with excellent chemoselectivities. Synthetic applications that showcase the possibilities of this novel methodology include an efficient one-pot synthesis of 4-aryl-4H-pyrans as well as the rapid construction of various heterocyclic, bicyclic, and polycyclic compounds.

Indexed as

conjugated enynesmonocarbonylationpalladiumP ligandsselectivity

Identifiers

PMID32052900
PMCPMC7317973

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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.