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Data · dataset · 2026

Visible-Light-Mediated Skeletal Editing of Furans to Pyridazines

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We herein describe a visible-light-mediated skeletal editing of furans to pyridazines via formal O-to-NN atom-pair exchange using hydrazine hydrate.

Description

The reaction proceeds under metal-free conditions at room temperature in air, providing di-, tri-, and tetrasubstituted pyridazines with complete regiocontrol from readily available furans. Broad functional-group tolerance, gram-scale synthesis, and late-stage skeletal editing of complex molecules are demonstrated.

Mechanistic studies suggest that water suppresses hydrazine-mediated quenching of the excited photocatalyst, while additional experiments support the involvement of oxygen-derived reactive species in the overall transformation.

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Provenance · 1 source records, 11 field assertions
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ZivaHuboai:figshare.com:article/340280589 d agoJSON v1
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