Macrocycle formation by ring-closing-metathesis. 2. An efficient synthesis of enantiomerically pure (R)-(+)-lasiodiplodin

This publication has 36 references indexed in Scilit:

• Conformationally Unbiased Macrocyclization Reactions by Ring Closing Metathesis
  The Journal of Organic Chemistry, 1996
• The First Catalytic Enantioselective Synthesis of (R)-(+) Lasiodiplodin
  Synlett, 1993
• Synthese von (R)‐Lasiodiplodin aus Polyhydroxybuttersäure
  European Journal of Organic Chemistry, 1990
• Asymmetric synthesis of orsellinic acid type macrolides: The example of lasiodiplodin
  Tetrahedron: Asymmetry, 1990
• Structure of arnebinol, a new ANSA-type monoterpenylbenzenoid with inhibitory effect to prostaglandin biosynthesis
  Tetrahedron Letters, 1983
• 2, 3‐Alkadiensäureester als Dienophile; Anwendung bei der Synthese von (+)‐(R)‐Lasiodiplodin
  Helvetica Chimica Acta, 1982
• Simple synthetic route to lasiodiplodin
  The Journal of Organic Chemistry, 1979
• A new synthetic method for aromatic type medium and large membered lactones based on intramolecular alkylation of ω-haloalkyl 2-phenylthiomethylbenzoate, and its application to the synthesis of (±)lasiodiplodin using a butadiene telomer
  Tetrahedron Letters, 1978
• 2‐(Trimethylsilyl)äthylester als Carboxylschutzgruppe; Anwendung bei der Synthese des (−)‐(S)‐Curvularins
  Helvetica Chimica Acta, 1977
• Synthese des (±)‐Lasiodiplodins
  Helvetica Chimica Acta, 1977