ArticleChemical science2022
Carbocation catalysis in confined space: activation of trityl chloride inside the hexameric resorcinarene capsule.
Article in Chemical science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
What it found
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Who cites it
6 citing papers in PubMed.
- Non-Dilute Synthesis of Macrodiolides and Macrotetrolides Enabled by Confinement Catalysis.Angewandte Chemie (International ed. in English) · 2026Article
- Exploring the formation of medium-sized cyclic amines within self-assembled yoctoliter inner-spaces.Chemical science · 2026Article
- Molecular Modeling Is Key to Understanding Supramolecular Resorcinarenyl Capsules, Inclusion Complex Formation and Organic Reactions in Nanoconfined Space.Molecules (Basel, Switzerland) · 2025Review
- Regioselective Dimerization of Methylcyclopentadiene inside Cucurbit[7]uril.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025Article
- The Versatile Applications of Calix[4]resorcinarene-Based Cavitands.Molecules (Basel, Switzerland) · 2024Review
- Insights into the Friedel-Crafts Benzoylation ofOrganic letters · 2023Article
Corrections and comments
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Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Carbocation catalysis can be performed inside the confined space of the hexameric resorcinarene capsule. The inner cavity of the capsule can host the trityl carbocation, which catalyses the Diels-Alder reaction between dienes and unsaturated aldehydes. Experimental results and
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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.