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Stereoselective Transformation of Phytosphingosine to Safingol

  • Kim, Na-Ri (Department of Chemistry, Seoul Women’s University) ;
  • Lee, Sun-Hee (Department of Chemistry, Seoul Women’s University) ;
  • Namgoong, Sung-Keon (Department of Chemistry, Seoul Women’s University)
  • Published : 2009.03.20

Abstract

A short and efficient synthesis of (2S,3S)-safingol from commercially available D-ribo-(2S,3S,4R)-phytosphingosine is described. The highlights of the synthesis are a stereoselective one-pot transformation of a diol into an epoxide under phase transfer catalytic conditions and a regioselective epoxide-opening reduction with a hydride reagent.

Keywords

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  4. ‘Chiron’ approach to stereoselective synthesis of sphinganine and unnatural safingol, an antineoplastic and antipsoriatic agent vol.6, pp.18, 2016, https://doi.org/10.1039/C5RA27342K
  5. - and Enantioselective Henry Reactions of Aliphatic Aldehydes and Application to the Synthesis of Safingol vol.19, pp.49, 2013, https://doi.org/10.1002/chem.201303650
  6. Stereoselective synthesis and antiproliferative activity of the isomeric sphinganine analogues vol.472, pp.None, 2019, https://doi.org/10.1016/j.carres.2018.09.008