Nucleophilic aromatic substitution by [18F]fluoride at substituted 2-nitropyridines
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[1] G. Reischl,et al. Nucleophilic substitution of nitro groups by [18F]fluoride in methoxy-substituted ortho-nitrobenzaldehydes—A systematic study , 2009 .
[2] G. Reischl,et al. Decarbonylation of multi-substituted [18F]benzaldehydes for modelling syntheses of 18F-labelled aromatic amino acids. , 2007, Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine.
[3] O. Mongin,et al. New syntheses of orelline and analogues via metalation and cross-coupling reactions , 2002 .
[4] C. Crouzel,et al. 2‐[18F]fluoropyridines by no‐carrier‐added nucleophilic aromatic substitution with [18F]FK‐K222—a comparative study , 1999 .
[5] R. Rengan,et al. Can we predict reactivity for aromatic nucleophilic substitution with [18F]fluoride ion? , 1993 .
[6] E. Breitmaier,et al. Carbon-13 NMR Spectroscopy: High-Resolution Methods and Applications in Organic Chemistry and Biochemistry , 1986 .
[7] K. Fukushi,et al. Synthesis of 18F-6-flouropurine and 18F-6-flouro-9-β-D-ribofuranosylpurine , 1982 .
[8] M. Schüller,et al. Synthesis, quality control and tissue distribution of 2-[18F]-nicotinic acid diethylamide, a potential agent for regional cerebral function studies , 1982 .