Catalytic strategies towards 1,3-polyol synthesis by enantioselective cascades creating multiple alcohol functions

Org Biomol Chem. 2020 Feb 14;18(6):1025-1035. doi: 10.1039/c9ob02675d. Epub 2020 Jan 24.

Abstract

This review highlights the different enantioselective catalyst-controlled cascades creating multiple alcohol functions through the formation of several carbon-carbon bonds. Through subsequent simple derivatization, these strategies ensure the rapid preparation of 1,3-polyols. Thanks to the use of efficient metal- or organo-catalysts, these cascades enable the selective assembly of multiple substrates considerably limiting operations and waste generation. For this purpose, several mono- or bi-directional approaches have been devised allowing successive C-C bond-forming events. The considerable synthetic economies these cascades enable have been demonstrated in the preparation of a wide variety of complex bioactive natural products, notably polyketides.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Alcohols / chemistry*
  • Catalysis
  • Molecular Structure
  • Polymers / chemical synthesis*
  • Polymers / chemistry
  • Stereoisomerism

Substances

  • Alcohols
  • Polymers
  • polyol