One-pot process that efficiently generates single stereoisomers of 1,3-bisphosphinylpropanes having five chiral centers

Org Lett. 2015 Jan 2;17(1):142-5. doi: 10.1021/ol503371r. Epub 2014 Dec 18.

Abstract

P,C-stereogenic 1,3-bisphosphinylpropanes 3 that have up to five stereogenic centers could be obtained stereoselectively in high yields by a one-step reaction of (RP)-menthylphenylphosphine oxide 1 with α,β-unsaturated aldehydes 2 catalyzed by KOH at room temperature. A mechanism was proposed as to involve a stereoselective intermolecular 1,3'-phosphorus migration from the 1,2-adduct of 1 with 2 to another 2 generating a 1,4-adduct that subsequently reacts with 1 to produce 3.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehydes / chemistry
  • Catalysis
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Phosphinic Acids / chemical synthesis*
  • Phosphinic Acids / chemistry
  • Propane / analogs & derivatives
  • Propane / chemical synthesis*
  • Propane / chemistry
  • Stereoisomerism

Substances

  • Aldehydes
  • Phosphinic Acids
  • Propane