Enzymatic Intra- and Intermolecular Hydroalkylations of Alkenes through Ground-State Electron Transfer

Key words

hydroalkylation - alkenes - reductase - ground-state electron transfer - ketones

Significance

Hyster and co-workers report intra- and intermolecular reductive hydroalkylations of aromatic olefins to form cyclopentanones or linear ketones in excellent yields and enantioselectivities. Quadruply mutated or wild-type nicotinamide-dependen­t cyclohexanone reductase (NCR), respectively, serve as efficient biocatalysts. Starting from α-bromo ketones, ground-state electron transfer from a flavinmononucleotide generates a ketyl radical that, through mesolytic C–Br bond cleavage, generates the reactive α-ketonyl radical. Notably, whereas the stereocenter in the cyclization reaction is set in the C–C bond-forming step, the enantiocontrol in intermolecular reactions originates from a stereoselective radical-terminating hydrogen-atom transfer.

Comment

Flavin-dependent ene-reductases (EREDs) have been previously applied in photo­enzymatic settings (see, for example: K. F. Biegasiewicz­ et al. Science 2019, 364, 1166). Whereas those reactions rely on the photoexcitation of a charge-transfer complex between enzyme, cofactor, and substrates, the analogous ground-state electron transfer had not previously been utilized as an initiation mechanism in C–C bond-forming reactions. The authors therefore selected α-bromo ketones as substrates due to their relatively high reduction­ potential, rendering ground-state reactivity­ kinetically feasible. Although the present method is an impressive example of enantiocontrol over real radical intermediates, the extension to less-stabilized nonaromatic substrates represents a considerable challenge for future research.

Publikationsverlauf

Artikel online veröffentlicht:
18. August 2021