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• W2091013485 abstract "A copper-catalyzed regio- and intermolecular aminofluorination of styrenes has been developed. In this reaction Ph-I=N-Ts and Et3N·3HF act as nitrogen and fluorine sources, respectively. The obtained β-fluoro-N-Ts-phenethylamines can be N-alkylated with subsequent deprotection affording the corresponding β-fluoro-N-alkylated phenethylamines, which are interesting building blocks for compounds acting on neuronal targets." @default.
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• W2091013485 date "2015-01-01" @default.
• W2091013485 modified "2023-10-01" @default.
• W2091013485 title "Copper-catalyzed intermolecular and regioselective aminofluorination of styrenes: facile access to β-fluoro-N-protected phenethylamines" @default.
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• W2091013485 doi "https://doi.org/10.1039/c4cc10162f" @default.
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