Enzymatic Bromocyclization of α- and γ-Allenols by Chloroperoxidase from Curvularia inaequalis

ChemistryOpen. 2022 Jan;11(1):e202100236. doi: 10.1002/open.202100236.

Abstract

Vanadate-dependent chloroperoxidase from Curvularia inaequalis catalyzes 5-endo-trig bromocyclizations of α-allenols to produce valuable halofunctionalized furans as versatile synthetic building blocks. In contrast to other haloperoxidases, also the more challenging 5-exo-trig halocyclizations of γ-allenols succeed with this system even though the scope still remains more narrow. Benefitting from the vanadate chloroperoxidase's high resiliency towards oxidative conditions, cyclization-inducing reactive hypohalite species are generated in situ from bromide salts and hydrogen peroxide. Crucial requirements for high conversions are aqueous biphasic emulsions as reaction media, stabilized by either cationic or non-ionic surfactants.

Keywords: allenes; cyclization; halogenation; haloperoxidase; heterocycles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chloride Peroxidase*
  • Curvularia
  • Vanadates

Substances

  • Vanadates
  • Chloride Peroxidase

Supplementary concepts

  • Curvularia inaequalis