[18F]Fluoroamines via ring-opening of N-Cbz-2-methylaziridine with [18F]-fluoride
摘要:
A highly regioselective method was developed for ring-opening benzyloxycarbonyl (Cbz)-protected 2-methylaziridine with [F-18]-labelled fluoride. Following catalytic hydrogenation, 1-[F-18]fluoro-2-propanamine([F-18]1) and 2-[F-18]flouro-1-\propanamine([F-18]2) were prepared as the major and minor products, respectively (85:15), and were characterized following acylation with benzyl chloride, This methodology is applicable towards the generation of new [F-18]-labelled amines for incorporation into radiopharmaceuticals. (c) 2008 Elsevier Ltd. All rights reserved.
Synthèse D'α,β-fluoroamines à partir d'aziridines : orientation de l'ouverture du cycle et amélioration du pouvoir fluorant du réactif de olah
作者:Gérard Alvernhe、Sylvie Lacombe、André Laurent
DOI:10.1016/s0040-4039(00)71192-0
日期:1980.1
Ring opening of aziridines by different fluorinating reagents: three synthetic routes to .alpha.,.beta.-fluoro amines with different stereochemical pathways
作者:Gerard M. Alvernhe、Christine M. Ennakoua、Sylvie M. Lacombe、Andre J. Laurent
DOI:10.1021/jo00337a024
日期:1981.11
ALVERNHE G.; LACOMBE S.; LAURENT A., TETRAHEDRON LETT., 1980, 21, NO 3, 289-292
作者:ALVERNHE G.、 LACOMBE S.、 LAURENT A.
DOI:——
日期:——
ALVERNHE, G. M.;ENNAKOUA, C. M.;LACOMBE, S. M.;LAURENT, A. J., J. ORG. CHEM., 1981, 46, N 24, 4938-4948
作者:ALVERNHE, G. M.、ENNAKOUA, C. M.、LACOMBE, S. M.、LAURENT, A. J.