2-Oxo promoted hydrophosphonylation & aerobic intramolecular nucleophilic displacement reaction

Org Biomol Chem. 2015 Aug 28;13(32):8637-41. doi: 10.1039/c5ob01310k. Epub 2015 Jul 23.

Abstract

Highly efficient catalyst free methods for the synthesis of α-hydroxy-β-oxophosphonates and α-oxoesters have been described. The existence of a 2-oxo group in α-oxoaldehydes is a key factor in promoting the reaction of the tervalent phosphite form towards 2-oxoaldehydes in the synthesis of α-hydroxy-β-oxophosphonates. The in situ activated α-C-H atom of α-hydroxy-β-oxophosphonates sustains aerobic intramolecular nucleophilic displacement in a curious way to produce α-oxoester.

MeSH terms

  • Aldehydes / chemistry
  • Esters / chemical synthesis*
  • Esters / chemistry
  • Molecular Structure
  • Organophosphonates / chemical synthesis*
  • Organophosphonates / chemistry
  • Phosphites / chemistry
  • Phosphorylation

Substances

  • Aldehydes
  • Esters
  • Organophosphonates
  • Phosphites