Divergent Total Syntheses of Rhodomyrtosones A and B

J Org Chem. 2015 Oct 2;80(19):9584-91. doi: 10.1021/acs.joc.5b01570.

Abstract

Herein, we report total syntheses of the tetramethyldihydroxanthene natural product rhodomyrtosone B and the related bis-furan β-triketone natural product rhodomyrtosone A. Nickel-(II)-catalyzed 1,4-conjugate addition of an α-alkylidene-β-dicarbonyl substrate was developed to access the congener rhodomyrtosone B, and oxygenation of the same monoalkylidene derivative followed by cyclization was employed to obtain the bis-furan natural product rhodomyrtosone A.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Products
  • Catalysis
  • Cyclization
  • Furans / chemistry*
  • Heterocyclic Compounds, 3-Ring / chemical synthesis*
  • Heterocyclic Compounds, 3-Ring / chemistry
  • Ketones / chemistry*
  • Molecular Structure
  • Nickel
  • Stereoisomerism

Substances

  • Biological Products
  • Furans
  • Heterocyclic Compounds, 3-Ring
  • Ketones
  • rhodomyrtosone A
  • rhodomyrtosone B
  • Nickel
  • furan