Complex of 4-Fluorophenol with α-Cyclodextrin: Binding Mode in Solution Is Opposite to That in the Solid State
Author:
Affiliation:
1. Department of Medicinal Chemistry, School of Pharmacy, State University of New York at Buffalo, Buffalo, New York 14260, and Roswell Park Cancer Institute, Department of Biophysics, Buffalo, New York 14263
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo970772m
Reference9 articles.
1. Crystallography of Supramolecular Compounds; NATO ASI Series C, No. 480; Kluwer Academic; Boston, 1996.
2. X-Ray crystallographic study of fluorine atom effect on guest orientation inside the α-cyclodextrin cavity
3. Conformational, calorimetric and NMR spectroscopic studies on inclusion complexes of cyclodextrins with substituted phenyl and adamantane derivatives
4. Djedaini, F.; Perly, B. InNew Trends in Cyclodextrins and Derivatives; Duchene, D., Ed.; Editions de Sante: Paris, 1991; Chapter 6, pp 215−246.
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