Divergent Strategy in Marine Tetracyclic Meroterpenoids Synthesis

Mar Drugs. 2021 May 13;19(5):273. doi: 10.3390/md19050273.

Abstract

The divergent total synthesis strategy can be successfully applied to the preparation of families of natural products using a common late-stage pluripotent intermediate. This approach is a powerful tool in organic synthesis as it offers opportunities for the efficient preparation of structurally related compounds. This article reviews the synthesis of the marine natural product aureol, as well as its use as a common intermediate in the divergent synthesis of other marine natural and non-natural tetracyclic meroterpenoids.

Keywords: aureol; divergent total synthesis; marine natural products; tetracyclic meroterpenoids.

Publication types

  • Review

MeSH terms

  • Animals
  • Aquatic Organisms / chemistry*
  • Biological Products / chemistry*
  • Biological Products / pharmacology
  • Heterocyclic Compounds, 4 or More Rings / chemical synthesis*
  • Heterocyclic Compounds, 4 or More Rings / chemistry
  • Sesquiterpenes / chemical synthesis*
  • Sesquiterpenes / chemistry
  • Terpenes / chemical synthesis*
  • Terpenes / chemistry

Substances

  • Biological Products
  • Heterocyclic Compounds, 4 or More Rings
  • Sesquiterpenes
  • Terpenes
  • aureol