Asymmetric organocatalytic synthesis of quaternary α-hydroxy phosphonates: en route to α-aryl phosphaisoserines

Chem Commun (Camb). 2015 Mar 7;51(19):4077-80. doi: 10.1039/c4cc10390d.

Abstract

The dual activation of acyl phosphonates and formaldehyde tert-butyl hydrazone by a BINAM-derived bis-urea catalyst is the key to achieve high reactivities and enantioselectivities in the synthesis of densely functionalized quaternary α-hydroxy phosphonates. Subsequent high-yielding transformations in a 'one-pot' fashion provide direct access to valuable azoxy compounds and quaternary α-aryl-phosphaisoserines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Chemistry Techniques, Synthetic
  • Formaldehyde / chemistry
  • Models, Molecular
  • Molecular Conformation
  • Organophosphonates / chemical synthesis*
  • Organophosphonates / chemistry*
  • Serine / analogs & derivatives*
  • Serine / chemistry
  • Stereoisomerism
  • Urea / chemistry

Substances

  • Organophosphonates
  • Formaldehyde
  • Serine
  • isoserine
  • Urea