Synlett 1991; 1991(9): 654-656
DOI: 10.1055/s-1991-20830
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 N-[1-(2-Thienyl)cyclohexyl]piperidine (TCP) Based Irreversible Alkylators of the Phenylcyclidine (PCP) Recognition Site

Alan P. Kozikowski* , Abdul H. Fauq, Werner Tückmantel, Stefano O. Casalotti, Karl E. Krueger
  • *Neurochemistry Research, Mayo Clinic Jacksonville, 4500 San Pablo Road, Jacksonville, Florida 32224, USA
Weitere Informationen

Publikationsverlauf

Publikationsdatum:
07. März 2002 (online)

Four new thienylcyclohexylamines {N-[1-(4-isothiocyanato/isoselenocyanato-2-thienyl)cyclohexyl]piperidine and 2-[1-(ethylaminocyclohexyl)-4-isothiocyanato/isoselenocyanatothiophene) have been synthesized and examined for their ability to alkylate the MK-801/PCP recognition sites associated with the N-methyl-D-aspartate receptor-ion channel complex.

    >