Binding of Acetylcholine and Quaternary Ammonium Cations to Macrocyclic and Acyclic “Phane” Esters. Evaluation of the Cation−π Primary Interaction through Adaptive Aromatic Hosts-Reference-Cited by-同舟云学术

Binding of Acetylcholine and Quaternary Ammonium Cations to Macrocyclic and Acyclic “Phane” Esters. Evaluation of the Cation−π Primary Interaction through Adaptive Aromatic Hosts

Published:1998-11-18 Issue:48 Volume:120 Page:12443-12452
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Roelens Stefano¹,Torriti Riccardo¹

Affiliation:

1. Contribution from the CNR, Centro di Studio sulla Chimica e la Struttura dei Composti Eterociclici e loro Applicazioni, Dipartimento di Chimica Organica, Università di Firenze, I-50121 Firenze, Italy

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja981338k

Reference46 articles.

1. The Cation−π Interaction

2. Cation-π Interactions in Chemistry and Biology: A New View of Benzene, Phe, Tyr, and Trp

3. Acetylcholine Binding by a Synthetic Receptor: Implications for Biological Recognition

4. "Hydrophobic" binding of water-soluble guests by high-symmetry, chiral hosts. An electron-rich receptor site with a general affinity for quaternary ammonium compounds and electron-deficient .pi. systems

5. Tight, oriented binding of an aliphatic guest by a new class of water-soluble molecules with hydrophobic binding sites

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