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Synthesis of non-symmetrical alkynylpyridines by chemoselective Sonogashira cross-coupling reactions

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Abstract 4-Bromo-2,3,5-trichloro-6-iodopyridine was studied as a new substrate in chemoselective Sonogashira reactions. This approach provides an efficient access to non-symmetrical mono-, di-, tri- and pentaalkynylated pyridines in good yields. Selected… Click to show full abstract

Abstract 4-Bromo-2,3,5-trichloro-6-iodopyridine was studied as a new substrate in chemoselective Sonogashira reactions. This approach provides an efficient access to non-symmetrical mono-, di-, tri- and pentaalkynylated pyridines in good yields. Selected pentaalkynylated pyridines were studied with regard to their UV/Vis- and emission properties showing moderate to high fluorescence quantum yields.

Keywords: synthesis non; non symmetrical; symmetrical alkynylpyridines; alkynylpyridines chemoselective; chemoselective sonogashira

Journal Title: Tetrahedron
Year Published: 2019

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