Evidence map›Paper›PMID 31283092›Full record

ReviewAngewandte Chemie (International ed. in English)2020

Regioselective Functionalization of [2.2]Paracyclophanes: Recent Synthetic Progress and Perspectives.

Zahid Hassan, Eduard Spuling, Daniel M Knoll, Stefan Bräse

Abstract readReview
In one paragraph

Review 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 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing 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

44 citing papers in PubMed.

  1. Article
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  4. Helical Dispiroindeno[2,1-The Journal of organic chemistry · 2026
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  5. Article
  6. Review
  7. Article
  8. Article
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  10. Synthesis of optically active folded cyclic dimers and trimers.Beilstein journal of organic chemistry · 2025
    Article
  11. Article
  12. Article
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  14. Article
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  16. Article
  17. Article
  18. Review
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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.

Zahid HassanInstitute of Organic Chemistry (IOC), Fritz-Haber-Weg 6, 76131, Karlsruhe, Germany.ORCID http://orcid.org/0000-0001-5011-9905
Eduard SpulingInstitute of Organic Chemistry (IOC), Fritz-Haber-Weg 6, 76131, Karlsruhe, Germany.ORCID http://orcid.org/0000-0002-6881-9018
Daniel M KnollInstitute of Organic Chemistry (IOC), Fritz-Haber-Weg 6, 76131, Karlsruhe, Germany.ORCID http://orcid.org/0000-0002-3592-1366
Stefan BräseInstitute of Organic Chemistry (IOC), Fritz-Haber-Weg 6, 76131, Karlsruhe, Germany.ORCID http://orcid.org/0000-0003-4845-3191

Funding

Deutsche Forschungsgemeinschaft SFB 1176 3DMM2O, TRR88
6 · The paper itself

Abstract

[2.2]Paracyclophane (PCP) is a prevalent scaffold that is widely utilized in asymmetric synthesis, π-stacked polymers, energy materials, and functional parylene coatings that finds broad applications in bio- and materials science. In the last few years, [2.2]paracyclophane chemistry has progressed tremendously, enabling the fine-tuning of its structural and functional properties. This Minireview highlights the most important recent synthetic developments in the selective functionalization of PCP that govern distinct features of planar chirality as well as chiroptical and optoelectronic properties. Special focus is given to the function-inspired design of [2.2]paracyclophane-based π-stacked conjugated materials by transition-metal-catalyzed cross-coupling reactions. Current synthetic challenges, limitations, as well as future research directions and new avenues for advancing cyclophane chemistry are also summarized.

Indexed as

[2.2]paracyclophaneschiralityfunctional parylenesregioselective synthesisπ-stacked polymers

Identifiers

PMID31283092
PMCPMC7003812

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.