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A facile diversity-oriented synthesis of imidazo[1,2-a]pyrazinones via?gold-catalyzed regioselective heteroannulation of propynylaminopyrazinones
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文摘
A gold-catalyzed regioselective heteroannulation strategy has been developed for the concise and efficient synthesis of imidazo[1,2-a]pyrazinones. The protocol allows the introduction of diversity via the application of substituted propargyl amines or via Suzuki-coupling of the generated imidazo[1,2-a]pyrazinones with various (het)aryl boronic acids.

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