Enantioselektive Synthese von Altohyrtin C (Spongistatin 2): Synthese der AB- und CD-Spiroketale

This publication has 37 references indexed in Scilit:

• A modular approach to marine macrolide construction. 1. An enantiocontrolled route to the C1–C12 (AB) spiroacetal sector
  Tetrahedron Letters, 1997
• Studies in marine macrolide synthesis: Stereocontrolled synthesis of the AB-spiroacetal subunit of spongistatin 1 (altohyrtin A)
  Tetrahedron Letters, 1996
• A Method for Constructing the C2−C12 Dispiroacetal Moiety of Altohyrtin A
  The Journal of Organic Chemistry, 1996
• Marine Natural Products. XXXVIII. Absolute Stereostructures of Altohyrtins A, B, and C and 5-Desacetylaltohyrtin A, Potent Cytotoxic Macrolides, from the Okinawan Marine Sponge Hyrtios altum.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1996
• Absolute stereostructures of altohyrtin A and its congeners, potent cytotoxic macrolides from the Okinawan marine sponge hyrtios altum
  Tetrahedron Letters, 1994
• Total synthesis of (+)-A83543A [(+)-lepicidin A]
  Journal of the American Chemical Society, 1993
• Bioactive marine metabolites. 48. Cinachyrolide A: a potent cytotoxic macrolide possessing two spiro ketals from marine sponge Cinachyra sp
  Journal of the American Chemical Society, 1993
• Altohyrtin A, a potent anti-tumor macrolide from the Okinawan marine sponge Hyrtios altum
  Tetrahedron Letters, 1993
• Antineoplastic agents. 257. Isolation and structure of spongistatin 1
  The Journal of Organic Chemistry, 1993
• Altohyrtins B and C and 5-desacetylaltohyrtin A, potent cytotoxic macrolide congeners of altohyrtin A, from the okinawan marine sponge Hyrtios altum.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1993