Chemoenzymatic, biomimetic total synthesis of (-)-rugulosin B, C and rugulin analogues and their biosynthetic implications

Chem Commun (Camb). 2020 Mar 17;56(22):3337-3340. doi: 10.1039/d0cc00406e.

Abstract

Herein, we report the chemoenzymatic synthesis of a heterodimeric (-)-rugulosin B, homodimeric (-)-rugulosin C, and several rugulin analogues in three to four steps starting from anthraquinones. This work supports dimerization between variously substituted putative monomeric intermediates during the biosynthesis of naturally occurring (+)-rugulosin B and C.

MeSH terms

  • Anthraquinones / chemical synthesis*
  • Anthraquinones / chemistry
  • Anthraquinones / metabolism
  • Biomimetics
  • Coordination Complexes / chemistry
  • Cycloaddition Reaction
  • Fungal Proteins / genetics
  • Fungal Proteins / metabolism
  • Lead / chemistry
  • Naphthoquinones / chemical synthesis
  • Naphthoquinones / chemistry*
  • Naphthoquinones / metabolism
  • Oxidation-Reduction
  • Oxidoreductases / genetics
  • Oxidoreductases / metabolism*
  • Talaromyces / enzymology

Substances

  • Anthraquinones
  • Coordination Complexes
  • Fungal Proteins
  • Naphthoquinones
  • rugulosin B
  • rugulosin C
  • Lead
  • rugulin
  • Oxidoreductases