Acetylcholinesterase inhibitory activities of muscarine and muscarone derivatives-Reference-Cited by-同舟云学术

Acetylcholinesterase inhibitory activities of muscarine and muscarone derivatives

Published:1959-08 Issue:8 Volume:15 Page:300-301
ISSN:0014-4754
Container-title:Experientia
language:en
Short-container-title:Experientia

Author:

Witkop B.,Durant R. C.,Friess S. L.

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Cellular and Molecular Neuroscience,Pharmacology,Molecular Biology,Molecular Medicine

Link

http://link.springer.com/content/pdf/10.1007/BF02158533.pdf

Reference8 articles.

1. The correct way to represent the absolute configuration ofl-muscarine [E. Hardegger andF. Lohse, Helv. chim. Acta40, 2383 (1957] is shown in I which pictures it as N-[1,3,6-trideoxy-2,5-anhydro-l-ribo-hexityl]-N-trimethylammonium halide. The Rosanov carbon is C(5) and has the LG-configuration.

2. C. H. Eugster, F. Häfliger, R. Denss, andE. Girod, Helv. chim. Acta41, 205, 583, 705 (1958); Helv. chim. Acta42 (1959), in press.

3. We are greatly indebted to Dr.F. Häfliger, J. R. Geigy, Basle, for placing these compounds at our disposal.

4. S. L. Friess, A. A. Patchett, andB. Witkop, J. Amer. chem. Soc.79, 459 (1957).

5. I. B. Wilson, J. biol. Chem.197, 215 (1952).

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