Evidence map›Paper›PMID 36545133›Full record

ReviewChemical science2022

Recent advances in the dearomative functionalisation of heteroarenes.

Nicolas Kratena, Bruno Marinic, Timothy J Donohoe

Abstract readReview
In one paragraph

Review in Chemical science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Oxidative Dearomatization of Pyridines.Journal of the American Chemical Society · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. 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

3 authors.

Nicolas KratenaChemistry Research Laboratory, University of Oxford 12 Mansfield Road Oxford OX1 3TA UK timothy.donohoe@chem.ox.ac.uk.ORCID https://orcid.org/0000-0002-3080-7214
Bruno MarinicChemistry Research Laboratory, University of Oxford 12 Mansfield Road Oxford OX1 3TA UK timothy.donohoe@chem.ox.ac.uk.ORCID https://orcid.org/0000-0003-0976-3373
Timothy J DonohoeChemistry Research Laboratory, University of Oxford 12 Mansfield Road Oxford OX1 3TA UK timothy.donohoe@chem.ox.ac.uk.ORCID https://orcid.org/0000-0001-7088-6626

Funding

Austrian Science Fund FWF J 4483
6 · The paper itself

Abstract

Dearomatisation reactions of (hetero)arenes have been widely employed as efficient methods to obtain highly substituted saturated cyclic compounds for over a century. In recent years, research in this area has shifted towards effecting additional C-C bond formation during the overall dearomative process. Moving away from classical hydrogenation-based strategies a wide range of reagents were found to be capable of initiating dearomatisation through nucleophilic addition (typically a reduction) or photochemically induced radical addition. The dearomatisation process gives rise to reactive intermediates which can be intercepted in an intra- or intermolecular fashion to deliver products with significantly increased molecular complexity when compared to simple dearomatisation. In this Perspective recent examples and strategies for the dearomative functionalisation of heteroaromatic systems will be discussed.

Identifiers

PMID36545133
PMCPMC9749106

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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.