Nucleophilic substitution at cyclic sulphamates—routes to NCA [18F]fluoro-analogues of MK 801-Reference-Cited by-同舟云学术

Nucleophilic substitution at cyclic sulphamates—routes to NCA [18F]fluoro-analogues of MK 801

Published:1989-01 Issue:4 Volume:40 Page:325-328
ISSN:0883-2889
Container-title:International Journal of Radiation Applications and Instrumentation. Part A. Applied Radiation and Isotopes
language:en
Short-container-title:International Journal of Radiation Applications and Instrumentation. Part A. Applied Radiation and Isotopes

Author:

Brady F.,Luthra S.K.,Pike V.W.

Publisher

Elsevier BV

Subject

General Engineering

Reference15 articles.

1. Quantitative autoradiography of [3H]-MK 801 binding sites in mammalian brain;Bowery;Br. J. Pharmacol.,1988

2. Stereospecific synthesis of N.C.A. 2-[18F]fluoro-2-deoxy-D-mannose and 2-[18F]-fluoro-2-deoxy-D-glucose and the influence of added carrier (KF) on FDG-synthesis;Hamacher;J. Labelled Compd. Radiopharm.,1986

3. Non-competitive antagonists of excitatory amino acid receptors;Kemp;Trends Neurosci.,1987

4. Lyle T.A. (1987) Personal communication

5. Fluoride-induced formation and ring-opening of cyclic sulfamates from hydroxy triflamides;Lyle;J. Am. Chem. Soc.,1987

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