Ring-closing metathesis as key step in the synthesis of Luffarin I, 16-epi-Luffarin I and Luffarin A

Mol Divers. 2016 May;20(2):369-77. doi: 10.1007/s11030-015-9638-7. Epub 2015 Oct 20.

Abstract

Natural sesterterpenolides, luffarin I and luffarin A, from Luffariella geometrica have been synthesized, and this is the first reported synthesis of luffarin A. The Yamaguchi esterification of the nor-diterpenic fragment, obtained from 2.8-15μM, with the appropriate furane alcohols yielded the necessary diene intermediates for the synthesis of the target molecules. The key strategic step in this synthesis was the ring-closing metathesis (RCM) reaction of the diene intermediates. This strategy allowed for the synthesis of 16-epi-luffarin I and analogues for structure-activity relationship (SAR) studies. The most active compound exhibited antiproliferative activity against a panel of six human solid tumour cell lines with [Formula: see text] values in the range 2.8-15 M.

Keywords: Cancer; Faulkner oxidation; Luffarins; Marine natural products; Ring-closing metathesis; Yamaguchi esterefication.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 4-Butyrolactone / analogs & derivatives*
  • 4-Butyrolactone / chemical synthesis
  • 4-Butyrolactone / chemistry
  • 4-Butyrolactone / pharmacology
  • Cell Line, Tumor
  • Cellular Reprogramming Techniques
  • Chemistry Techniques, Synthetic
  • Humans
  • Sesterterpenes / chemical synthesis*
  • Sesterterpenes / chemistry*
  • Sesterterpenes / pharmacology
  • Stereoisomerism

Substances

  • Sesterterpenes
  • luffarin A
  • luffarin I
  • 4-Butyrolactone