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Synthetic and conformational aspects of trimethylammonium-methyl substituted 2-oxazolines as potential cholinergics
Authors:Upinder Fotadar   Chris Becu   Frans A. M. Borremans  Marc J. O. Anteunis
Affiliation:

Department of Organic Chemistry, NMR-Spectroscopic Unit, Rijksuniversiteit-Gent, Krijgslaan 271 (S4bis), B-9000 Gent, Belgium

Abstract:The effects of some structural features on the cholinergic activity of 2-oxazoline derivatives has been investigated. Improved synthetic approaches to the 2-oxazoline ring system are developed, and several new fluorinated 2-oxazolines are described. The extensive NMR data give insight into the rotameric behaviour of the substituents.
Keywords:Present address: Department of Medicinal Chemistry   School of Pharmacy   University of Kansas/Laurence   KS 66045   U.S.A..
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