Total Synthesis of the Proposed Structure of Paraphaeosphaeride C

Molecules. 2019 Nov 21;24(23):4230. doi: 10.3390/molecules24234230.

Abstract

Paraphaeosphaeride C is a demethoxy derivative of phaeosphaeride A and exhibits STAT3 inhibitory activity. Our previous papers reported the total synthesis of phaeosphaeride A using a diastereoselective vinyl anion aldol reaction as the key step to construct the dihydropyran ring. In this work, the first total synthesis of the proposed structure of paraphaeosphaeride C was achieved via a similar synthetic strategy. The synthetic compound was characterized through extensive nuclear magnetic resonance (NMR) analysis but the 1H and 13C-NMR data for this compound did not correspond to those reported in the literature for paraphaeosphaeride C.

Keywords: STAT3; anti-cancer; paraphaeosphaeride C; stereoselective synthesis; total synthesis.

MeSH terms

  • Lactams / chemical synthesis*
  • Lactams / chemistry
  • Models, Molecular
  • Molecular Structure
  • Pyrones / chemical synthesis*
  • Pyrones / chemistry
  • Stereoisomerism

Substances

  • Lactams
  • Pyrones
  • paraphaeosphaeride C