Issue 21, 1995

Cation-π interaction between the trimethylammonium moiety and the aromatic ring within lndole-3-acetic acid choline ester, a model compound for molecular recognition between acetylcholine and its esterase: an X-ray study

Abstract

X-Ray analysis of indole-3-acetic acid choline ester, a model compound for molecular recognition between the neurotransmitter acetylcholine and its esterase, shows that the quaternary trimethylammonium group is folded back to make a close contact with the indole ring through the cation–π interaction; 1H NMR spectroscopy confirms this type of interaction also occurs in solution.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1995, 2221-2222

Cation-π interaction between the trimethylammonium moiety and the aromatic ring within lndole-3-acetic acid choline ester, a model compound for molecular recognition between acetylcholine and its esterase: an X-ray study

K. Aoki, K. Murayama and H. Nishiyama, J. Chem. Soc., Chem. Commun., 1995, 2221 DOI: 10.1039/C39950002221

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements