
Bioorganic and Medicinal Chemistry Letters p. 807 - 810 (1996)
Update date:2022-09-26
Topics:
Bowen, Tom
Planalp, Roy P.
Brechbiel, Martin W.
An improved synthesis of cis,cis-1,3,5-triaminocyclohexane in 82% yield involves reaction of the commercially available cis,cis-1,3,5-cyclohexanetricarboxylic acid with DPPA to afford the tri(benzylcarbamate) as the Curtius rearrangement product. Deprotection yields the triamine which serves as a platform from which a variety of chelating structures may be assembled. Novel tris(2-methylenepyridyl)triamine and tris(2-methylenethienyl)triamine ligands are prepared to investigate their suitability for use as gallium radiopharmaceuticals.
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Doi:10.1016/0040-4020(96)00453-X
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