Chemoenzymatic Synthesis of 3-Halochromones via Oxidative α-Halogenation of Enaminones in TPGS-750-M Micelles.

Abstract

Synthesis strategies of chromones have been widely investigated due to the abundance of chromone moiety in bioactive compounds and natural products. Of which, 3-halochromones are a versatile set of precursors to synthetically access valuable compounds with chromone frameworks. Generally, 3-halochromones were synthesized from o-hydroxy enaminones through oxidative α-halogenation, a process that often uses toxic and corrosive chemicals. Herein, we present an alternative strategy of oxidative α-halogenation catalyzed by vanadium-dependent chloroperoxidase from Curvularia inaequalis (CiVCPO) with H2O2/KX (X = Cl, Br, and I) in an aqueous medium. With a micellar system from a surfactant TPGS-750-M, substrate concentration can be increased to 50 mM without compromising the yield, thereby significantly reducing the use of organic solvents. Substrate scope investigation revealed that bromination and chlorination processes prefer electron-donating substituents although moderate electron-withdrawing groups were tolerated (20 examples). Additionally, iodination processes can be performed under the optimized condition. However, slow conversion indicated that further optimization is needed. We also found that iodination can occur without CiVCPO, albeit at a lower conversion. Further investigation suggested that such a conversion took place via I2 generated in situ. Overall, this chemoenzymatic method could offer an environmentally friendly approach to access a variety of 3-bromo or 3-chlorochromones.