Synthesis of geminal bisphosphonates via organocatalyzed enantioselective Michael additions of cyclic ketones and 4-piperidones

Org Biomol Chem. 2012 Jan 14;10(2):404-12. doi: 10.1039/c1ob06473h. Epub 2011 Nov 15.

Abstract

A Michael addition reaction of cyclic ketones and piperidones to a vinyl phosphonate is described. The reaction, catalyzed by chiral diamines, produced geminal γ-oxobisphosphonates in high yields (up to 92%) and very high ees (up to >99%). Disubstituted ketones gave drs of up to 8 : 92. The synthesis and characterization of several new compounds with potential biological activity is described.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Diamines / chemistry*
  • Diphosphonates / chemical synthesis*
  • Diphosphonates / chemistry
  • Ketones / chemistry*
  • Molecular Structure
  • Piperidones / chemistry*
  • Stereoisomerism

Substances

  • Diamines
  • Diphosphonates
  • Ketones
  • Piperidones