Total Synthesis of Apicularen A through Transannular Pyran Formation

This publication has 35 references indexed in Scilit:

• Total Synthesis and Biological Evaluation of (−)Apicularen A and Analogues Thereof
  Chemistry – A European Journal, 2003
• Chemistry and Biology of Salicylihalamide A and Related Compounds
  Chemical Reviews, 2003
• Induction of apoptosis of RAW 264.7 cells by the cytostatic macrolide apicularen A
  Journal of Pharmacy and Pharmacology, 2003
• Novel Marine and Microbial Natural Product Inhibitors of Vacuolar ATPase
  Current Medicinal Chemistry, 2003
• Stereocontrolled Total Synthesis of Apicularen A and Its Δ17,18Z Isomer
  Angewandte Chemie, 2002
• Stereocontrolled Total Synthesis of Apicularen A and Its Δ17,18 Z Isomer
  Angewandte Chemie International Edition in English, 2002
• Total synthesis and biological evaluation of apicularen A and synthetic analogs
  Tetrahedron Letters, 2001
• Apicularen A and B, Cytotoxic 10-Membered Lactones with a Novel Mechanism of Action fromChondromyces Species (Myxobacteria): Isolation, Structure Elucidation, and Biosynthesis
  European Journal of Organic Chemistry, 2000
• Apicularens A and B, New Cytostatic Macrolides from Chondromyces Species (Myxobacteria): Production, Physico-chemical and Biological Properties.
  The Journal of Antibiotics, 1998
• Salicylihalamides A and B, Novel Cytotoxic Macrolides from the Marine Sponge Haliclona sp.
  The Journal of Organic Chemistry, 1997