Evidence map›Paper›PMID 35191558›Full record

ReviewChemistry (Weinheim an der Bergstrasse, Germany)2022

Asymmetric Synthesis of Axially Chiral C-N Atropisomers.

Patricia Rodríguez-Salamanca, Rosario Fernández, Valentín Hornillos, José M Lassaletta

Abstract readReview
In one paragraph

Review 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 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed.

  1. Article
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  3. Article
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  5. Article
  6. Article
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  8. Article
  9. Rh-Catalyzed Atroposelective Single-Carbon Insertion.Journal of the American Chemical Society · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Atroposelective catalysis.Nature reviews. Chemistry · 2024
    Review
  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

4 authors.

Patricia Rodríguez-SalamancaInstituto de Investigaciones Químicas (CSIC-US) and Centro de, Innovación en Química Avanzada (ORFEO-CINQA), C/ Américo Vespucio, 49, 41092, Sevilla, Spain.
Rosario FernándezDepartamento de Química Orgánica, Universidad de Sevilla) and Centro de Innovación en Química Avanzada (ORFEO-CINQA) C/ Prof. García González, 1, 41012, Sevilla, Spain.
Valentín HornillosInstituto de Investigaciones Químicas (CSIC-US) and Centro de, Innovación en Química Avanzada (ORFEO-CINQA), C/ Américo Vespucio, 49, 41092, Sevilla, Spain.
José M LassalettaInstituto de Investigaciones Químicas (CSIC-US) and Centro de, Innovación en Química Avanzada (ORFEO-CINQA), C/ Américo Vespucio, 49, 41092, Sevilla, Spain.

Funding

Junta de Andalucía P18-FR-3531Junta de Andalucía P18-FR-644Ministerio de Ciencia e Innovación BES-2017-081561Ministerio de Ciencia e Innovación PID2019-106358GB-C21Ministerio de Ciencia e Innovación PID2019-106358GB-C22Ministerio de Ciencia e Innovación RYC-2017-22294Universidad de Sevilla US-1260906Universidad de Sevilla US-1262867
6 · The paper itself

Abstract

Molecules with restricted rotation around a single bond or atropisomers are found in a wide number of natural products and bioactive molecules as well as in chiral ligands for asymmetric catalysis and smart materials. Although most of these compounds are biaryls and heterobiaryls displaying a C-C stereogenic axis, there is a growing interest in less common and more challenging axially chiral C-N atropisomers. This review offers an overview of the various methodologies available for their asymmetric synthesis. A brief introduction is initially given to contextualize these axially chiral skeletons, including a historical background and examples of natural products containing axially chiral C-N axes. The preparation of different families of C-N based atropisomers is then presented from anilides to chiral five- and six-membered ring heterocycles. Special emphasis has been given to modern catalytic asymmetric strategies over the past decade for the synthesis of these chiral scaffolds. Applications of these methods to the preparation of natural products and biologically active molecules will be highlighted along the text.

Indexed as

Biological ProductsCatalysisLigandsStereoisomerismBiological ProductsLigands

Identifiers

PMID35191558
PMCPMC9314733

What OpenQuestion holds

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LicenceCC BY-NC
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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.