Synlett 1999; 1999(S1): 966-968
DOI: 10.1055/s-1999-3095
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Synthesis of a Chiral Receptor Molecule with Converging Amidinium and Hydroxy Groups

Tilmann Schuster* , Michael W. Göbel
  • *Institut für Organische Chemie der Johann Wolfgang Goethe-Universität, Marie-Curie-Strasse 11, D-60439 Frankfurt am Main, Germany; Fax +49(69)79 82 94 64; E-mail: M.Goebel@chemie.uni-frankfurt.de
Further Information

Publication History

Publication Date:
31 December 1999 (online)

The axially chiral amidinium ion 1 was synthesized by Suzuki cross coupling and by base induced cyclization of an amino nitrile intermediate. Receptor 1 may interact with guest molecules by three converging H-bond donors.