Formation of gamma-lactones through CAN-mediated oxidative cleavage of hemiketals.

Academic Article

Abstract

  • The generation of substituted gamma-lactones can be accomplished through application of a tandem chain extension-aldol reaction, followed by CAN-mediated oxidative cleavage of the aldol product. The oxidative cleavage requires the intermediacy of a hemiketal and the presence of an alpha-heteroatom. Formation of the gamma-lactone through the oxidative cleavage is used to assign stereochemistry of the aldol reaction and as the final step in a short synthesis of members of the phaseolinic acid family of natural products.
  • Authors

  • Jacobine, Alexander M
  • Lin, Weimin
  • Walls, Bethany
  • Zercher, Charles
  • Status

    Publication Date

  • September 19, 2008
  • Published In

    Keywords

  • 4-Butyrolactone
  • Cerium
  • Ketones
  • Lactones
  • Molecular Conformation
  • Oxidation-Reduction
  • Stereoisomerism
  • Digital Object Identifier (doi)

    Pubmed Id

  • 18693768
  • Start Page

  • 7409
  • End Page

  • 7412
  • Volume

  • 73
  • Issue

  • 18