Emergence of diversity and stereochemical outcomes in the biosynthetic pathways of cyclobutane-centered marine alkaloid dimers

Nat Prod Rep. 2016 Jul 28;33(7):820-42. doi: 10.1039/c5np00159e. Epub 2016 May 25.

Abstract

Covering: up to 2016Dictazoles and sceptrins are singular metabolites of marine origin. The present dichotomic case study provides a comprehensive perspective on these cyclobutane-centered alkaloids and their respective families. Indeed, their upstream and downstream chemistry are both treated herein. Relevant isolation reports and bio-inspired total syntheses are used to decipher the currently admitted biosynthetic hypotheses as well as the emergence of diversity in the two series. This review proposes a transversal vision of the topic, where most aspects of natural product chemistry have a critical importance.

Publication types

  • Review

MeSH terms

  • Biological Products / chemistry*
  • Biosynthetic Pathways
  • Cyclobutanes / chemistry*
  • Indole Alkaloids / chemistry*
  • Marine Biology*
  • Molecular Structure
  • Pyrroles / chemistry*

Substances

  • Biological Products
  • Cyclobutanes
  • Indole Alkaloids
  • Pyrroles
  • sceptrin