Synthesis of both 2,3-erythro- and 2,3-threo- isomers of aplidiasphingosine, a bioactive marine terpenoid

This publication has 10 references indexed in Scilit:

• Determination of the absolute configuration at C-6 and C-7 of serricornin (4,6-dimethyl-7-hydroxy-3-nonanone), the sex pheromone of the cigarette beetle
  Tetrahedron Letters, 1981
• Use of the E-vinyloxyborane derived from S-phenyl propanethioate for stereospecific aldol-type condensation. A simplified synthesis of the prelog-djerassi lactonic acid
  Tetrahedron Letters, 1979
• Acyclic stereoselection. 4. Assignment of stereostructure to .beta.-hydroxycarbonyl compounds by carbon-13 nuclear magnetic resonance
  The Journal of Organic Chemistry, 1979
• Aplidiasphingosine, an antimicrobial and antitumor terpenoid from an Aplidium species (marine tunicate)
  Journal of the American Chemical Society, 1978
• Pyridinium p-toluenesulfonate. A mild and efficient catalyst for the tetrahydropyranylation of alcohols
  The Journal of Organic Chemistry, 1977
• A new general method for protection of the hydroxyl function
  Tetrahedron Letters, 1976
• Synthesis of the Valeriana waalichi hydrocarbon sesquifenchene. Route to specifically functionalized 7,7-disubstituted bicyclo[2.2.1]heptane derivatives
  The Journal of Organic Chemistry, 1975
• A New, Highly Stereoselective Synthesis of alltrans-Geranylgeraniol
  Synthesis, 1974
• Improved aldehyde synthesis from 1,3-dithianes
  The Journal of Organic Chemistry, 1971
• Die Synthese des Sphingosins und seiner Stereoisomeren
  Helvetica Chimica Acta, 1957