Chemoenzymatic synthesis of (S)-eicos-(4E)-en-1-yn-3-ol, the cytotoxic principle of the marine sponge, Cribrochalina vasculum

This publication has 13 references indexed in Scilit:

• Novel antiproliferative falcarindiol furanocoumarin ethers from the root of Angelica japonica
  Bioorganic & Medicinal Chemistry Letters, 1998
• The absolute stereostructures of the polyacetylenic constituents of Ginseng Radix Rubra
  Tetrahedron, 1997
• Enzymatic resolution of alkyn-3-ols in non-aqueous medium
  Biotechnology Letters, 1996
• Antitumor Activity and Stereochemistry of Acetylenic Alcohols from the Sponge Cribrochalina vasculum
  Journal of Natural Products, 1995
• New acetylenic alcohols from the sponge Cribrochalina vasculum
  The Journal of Organic Chemistry, 1990
• Chiral Synthesis of Trogodermal, the Pheromone of Dermestid Beetles
  Synthetic Communications, 1990
• Melynes, polyacetylene constituents from a vanuatu marine sponge
  Tetrahedron Letters, 1988
• Bioactive marine metabolites XX. Petrosynol and petrosynone, antimicrobial C30 polyacetylenes from the marine sponge sp.: Determination of the absolute configuration
  Tetrahedron Letters, 1987
• H,K-ATPase inhibitors from the marine sponge : Absolute configuration of siphonodiol and two related metabolites
  Tetrahedron Letters, 1987
• New acetylenic compounds from the sponge reniera fulva
  Tetrahedron Letters, 1977