A multifunctional catalyst that stereoselectively assembles prodrugs

Science. 2017 Apr 28;356(6336):426-430. doi: 10.1126/science.aam7936.

Abstract

The catalytic stereoselective synthesis of compounds with chiral phosphorus centers remains an unsolved problem. State-of-the-art methods rely on resolution or stoichiometric chiral auxiliaries. Phosphoramidate prodrugs are a critical component of pronucleotide (ProTide) therapies used in the treatment of viral disease and cancer. Here we describe the development of a catalytic stereoselective method for the installation of phosphorus-stereogenic phosphoramidates to nucleosides through a dynamic stereoselective process. Detailed mechanistic studies and computational modeling led to the rational design of a multifunctional catalyst that enables stereoselectivity as high as 99:1.

MeSH terms

  • Amides / chemical synthesis*
  • Antineoplastic Agents / chemical synthesis*
  • Antiviral Agents / chemical synthesis*
  • Catalysis
  • Computer Simulation
  • Nucleosides / chemical synthesis*
  • Phosphoric Acids / chemical synthesis*
  • Prodrugs / chemical synthesis*
  • Stereoisomerism

Substances

  • Amides
  • Antineoplastic Agents
  • Antiviral Agents
  • Nucleosides
  • Phosphoric Acids
  • Prodrugs
  • phosphoramidic acid