Unified synthesis of tirandamycins and streptolydigins

Chem Commun (Camb). 2015 Dec 11;51(95):17004-7. doi: 10.1039/c5cc07749d.

Abstract

The asymmetric total syntheses of tirandamycins A-D and tirandalydigin as well as the synthesis of the left-hand fragment of streptolydiginone and streptolydigin from a common intermediate are described. The comprehensive approach features the highly enantio- and diastereoselective assembly of the anti,anti,syn-stereotetrad unit which relies on a cinchona alkaloid-catalyzed asymmetric Morita-Baylis-Hillman reaction.

MeSH terms

  • Aminoglycosides / chemical synthesis*
  • Anti-Bacterial Agents / chemical synthesis*
  • Bridged Bicyclo Compounds, Heterocyclic / chemical synthesis*
  • Hydrogenation
  • Pyrrolidinones / chemical synthesis*
  • Stereoisomerism

Substances

  • Aminoglycosides
  • Anti-Bacterial Agents
  • Bridged Bicyclo Compounds, Heterocyclic
  • Pyrrolidinones
  • tirandamycin C
  • tirandamycin D
  • tirandalydigin
  • tirandamycin A
  • tirandamycin B