ArticleJournal of the American Chemical Society2021
Diastereoselective Amplification of a Mechanically Chiral [2]Catenane.
Article in Journal of the American Chemical Society, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.
What it found
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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.
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Who cites it
14 citing papers in PubMed.
- Supramolecular self-assembly by layering orthogonality to program identity, connectivity and conformation.Nature reviews. Chemistry · 2026Review
- Cooperative reversible assembly in triply interlocked AlChemical science · 2025Article
- Effective RNA Complexation by [2]Catenanes Confers Enhanced Resistance to Enzymatic Degradation.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025Article
- Dynamic mechanostereochemical switching of a co-conformationally flexible [2]catenane controlled by specific ionic guests.Nature communications · 2024Article
- Article
- Dynamic covalent synthesis.Chemical science · 2024Review
- A catenane that is topologically achiral despite being composed of oriented rings.Nature chemistry · 2023Article
- Two-ring chirality generated by the alignment of two achiral phenylacetylene macrocycles.RSC advances · 2023Article
- Chiral Amplification through the Interplay of Racemizing Conditions and Asymmetric Crystal Growth.Journal of the American Chemical Society · 2023Article
- Knotting matters: orderly molecular entanglements.Chemical Society reviews · 2022Review
- Mechanically axially chiral catenanes and noncanonical mechanically axially chiral rotaxanes.Nature chemistry · 2022Article
- A Co-conformationally "Topologically" Chiral Catenane.Journal of the American Chemical Society · 2022Article
- Distinctive features and challenges in catenane chemistry.Chemical science · 2022Review
- Rotaxanes with dynamic mechanical chirality: Systematic studies on synthesis, enantiomer separation, racemization, and chiral-prochiral interconversion.Frontiers in chemistry · 2022Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Achiral [2]catenanes composed of rings with inequivalent sides may adopt chiral co-conformations. Their stereochemistry depends on the relative orientation of the interlocked rings and can be controlled by sterics or an external stimulus (e.g., a chemical stimulus). Herein, we have exploited this stereodynamic property to amplify a mechanically chiral (
Identifiers
What OpenQuestion holds
Registered trials
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.