Manik Sharma, Yue Li, Kirklin L. McWhorter, Tiffany V. Alvarez, Lorenzo Layug, Abbas Khambatti, Katherine M. Davis, Kyle F. Biegasiewicz
Diazo compounds are privileged carbene precursors in synthetic organic chemistry. Despite their versatility in both chemo- and biocatalytic chemical synthesis, their preparation typically requires the use of reagents that are expensive, toxic, and unsustainable. Herein, we describe a chemoenzymatic strategy for the preparation of stabilized diazo compounds enabled by enzymatic halide recycling with vanadium-dependent haloperoxidase (VHPO) enzymes. The process involves the conversion of a carbonyl-containing compound to an intermediate hydrazone that is subjected directly to a VHPO-catalyzed nitrogen-nitrogen (N-N) bond oxidation to afford the corresponding diazo compound. The protocol is applied to a broad range of carbonyls with moderate to high yield and excellent chemoselectivity. A series of molecular docking, molecular dynamics, microscale thermophoresis, and mutagenesis experiments provide insight into reactivity rate differences between (E)- and (Z)-configured hydrazones in the VHPO-mediated oxidation process. Finally, the developed method is interfaced with lipase-mediated transacylation to produce a collection of diazo derivatives starting from a single benzoylformate starting material.