Evidence map›Paper›PMID 35638452›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2022

Synthesis of 3,4-Dihydro-2H-Pyrroles from Ketones, Aldehydes, and Nitro Alkanes via Hydrogenative Cyclization.

Barbara Klausfelder, Patricia Blach, Niels de Jonge, Rhett Kempe

Abstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Synthesis of ΔACS omega · 2025
    Article
  2. 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

4 authors.

Barbara KlausfelderAnorganische Chemie II, Catalyst Design, Sustainable Chemistry Centre, University of Bayreuth, Universitätsstraße 30, 95440, Bayreuth, Germany.
Patricia BlachINM - Leibniz Institute for New Materials, Campus D2 2, 66123, Saarbrücken, Germany.
Niels de JongeINM - Leibniz Institute for New Materials, Campus D2 2, 66123, Saarbrücken, Germany.
Rhett KempeAnorganische Chemie II, Catalyst Design, Sustainable Chemistry Centre, University of Bayreuth, Universitätsstraße 30, 95440, Bayreuth, Germany.ORCID http://orcid.org/0000-0002-9138-4155

Funding

Deutsche Forschungsgemeinschaft KE 756 34-1
6 · The paper itself

Abstract

Syntheses of N-heterocyclic compounds that permit a flexible introduction of various substitution patterns by using inexpensive and diversely available starting materials are highly desirable. Easy to handle and reusable catalysts based on earth-abundant metals are especially attractive for these syntheses. We report here on the synthesis of 3,4-dihydro-2H-pyrroles via the hydrogenation and cyclization of nitro ketones. The latter are easily accessible from three components: a ketone, an aldehyde and a nitroalkane. Our reaction has a broad scope and 23 of the 33 products synthesized are compounds which have not yet been reported. The key to the general hydrogenation/cyclization reaction is a highly active, selective and reusable nickel catalyst, which was identified from a library of 24 earth-abundant metal catalysts.

Indexed as

AldehydesKetonesAlkanesCatalysisCyclizationMetalsPyrrolesAldehydesAlkanesKetonesMetalsPyrrolescatalysishydrogenationmulticomponent reactionN-heterocyclesnickel

Identifiers

PMID35638452
PMCPMC9545131

What OpenQuestion holds

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LicenceCC BY
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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.