Biomimetic synthesis of thiaplidiaquinones A and B

J Nat Prod. 2012 Dec 28;75(12):2256-60. doi: 10.1021/np300790g. Epub 2012 Dec 10.

Abstract

A biomimetic synthesis of the biologically active ascidian metabolites thiaplidiaquinones A and B is described. Reaction of geranylbenzoquinone with Et(3)N in CH(2)Cl(2) yielded two isomeric quinones, comprising the benzo[c]chromene-7,10-dione core of the natural products. Subsequent reaction with hypotaurine yielded the title compounds and their dioxothiazino regioisomers.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomimetics
  • Molecular Structure
  • Stereoisomerism
  • Terpenes / chemical synthesis
  • Terpenes / chemistry*
  • Urochordata / chemistry*

Substances

  • Terpenes
  • thiaplidiaquinone A
  • thiaplidiaquinone B