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(.+-.)-3-Allyl-7-halo-8-hydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepines as selective high affinity D1 dopamine receptor antagonists: synthesis and structure-activity relationship

โœ Scribed by Baindur, Nandkishore; Tran, Mai; Niznik, Hyman B.; Guan, H. C.; Seeman, Phillip; Neumeyer, John L.


Book ID
125960836
Publisher
American Chemical Society
Year
1992
Tongue
English
Weight
887 KB
Volume
35
Category
Article
ISSN
0022-2623

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โœ Hayden T. Ravert; Alan A. Wilson; Robert F. Dannals; Dean F. Wong; Henry N. Wagn ๐Ÿ“‚ Article ๐Ÿ“… 1987 ๐Ÿ› Elsevier Science โš– 200 KB

Carbon-11 labeled SCH 23390, a selective dopamine D-1 receptor antagonist (Fig. 1b), was prepared by N-alkylation of the nor-methyl precursor with [11C]iodomethane. The product was purified by semi-preparative HPLC and shown to be radiochemically pure at the end of synthesis. The synthesis was compl