Abstract
A Cu-catalyzed, one-pot synthesis of 1,2,3-triazolyl phenylethylamine scaffolds is reported. This method utilizes a single copper catalyst to promote aziridination via nitrene, ring opening with azide, and CuAAC to afford 1,4-disubstituted 1,2,3-triazole phenylethylamine scaffolds. The utility of this process is demonstrated in the synthesis of pharmaceutically relevant cores from simple styrene motifs.
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Supporting information
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Experimental procedures, charaterisation data, copies of spectra
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Checkcif file
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cif
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cif file
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Raw data files
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Raw NMR data output files obtained from Bruker Topspin® files as .zip folders, openable with suitable NMR processing software, such as Bruker Topspin® or MestReNova
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