An enantio- and stereo-controlled synthesis ofL-erythro- andD-threo-C₁₈-sphingosines via the anomalous version of the katsuki–sharpless asymmetric epoxidation reaction

This publication has 14 references indexed in Scilit:

• Inversion of enantioselectivity in the kinetic resolution mode of the Katsuki-Sharpless asymmetric epoxidation reaction
  Journal of the American Chemical Society, 1991
• Synthesis of fluorine-containing isosteres of sphingosine as inactivators of protein kinase C
  Tetrahedron Letters, 1990
• Stereochemistry associated with the addition of 2-(trimethylsilyl)thiazole to differentially protected .alpha.-amino aldehydes. Applications toward the synthesis of amino sugars and sphingosines
  The Journal of Organic Chemistry, 1990
• Total synthesis of (+)-erythro-N-lauroyldocosasphinga-4,8-dienine from Anemonia sulcata and determination of the absolute configuration
  Journal of the Chemical Society, Chemical Communications, 1990
• Synthesis of two pairs of enantiomeric C18-sphingosines
  Tetrahedron Letters, 1989
• Structural requirements for long-chain (sphingoid) base inhibition of protein kinase C in vitro and for the cellular effects of these compounds
  Biochemistry, 1989
• Synthesis of cerebroside B1b with antiulcerogenic activity I. Synthesis of ceramides with optically active α-hydroxypalmitic acids.
  Tetrahedron, 1989
• Glycosphingolipids
  Scientific American, 1986
• On the Mechanism of Asymmetric Epoxidation with Titanium—Tartrate Catalysts
  Published by Elsevier ,1985
• The first practical method for asymmetric epoxidation
  Journal of the American Chemical Society, 1980