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Base-Promoted 1,6-Aza-Michael Addition of Azauracils to para-Quinone Methides

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Here, we report an efficient higher order conjugate addition of azauracils to substituted para-Quinone methides (p-QMs) mediated by triethylamine to furnish hitherto unknown diarylmethane scaffolds through construction of a C-N… Click to show full abstract

Here, we report an efficient higher order conjugate addition of azauracils to substituted para-Quinone methides (p-QMs) mediated by triethylamine to furnish hitherto unknown diarylmethane scaffolds through construction of a C-N bond. The protocol features mild conditions, high atom economy, and broad scope, and enables convenient access to biologically relevant new chemical entities (NCEs) comprising p-QM and azauracil hybrid in good to excellent yields.

Keywords: base promoted; addition azauracils; para quinone; promoted aza; quinone methides

Journal Title: Synthesis
Year Published: 2023

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