First stereoselective total synthesis of antibiotic macrolide Berkeleylactone F

This publication has 28 references indexed in Scilit:

• The Berkeleylactones, Antibiotic Macrolides from Fungal Coculture
  Journal of Natural Products, 2017
• The first stereoselective total synthesis of the Z-isomer of (6S,7R,9R)-6,7-dihydroxy-9-propylnon-4-eno-9-lactone
  RSC Advances, 2013
• Titanium(IV)-Promoted Regioselective Nucleophilic Ring-Opening Reaction of Chiral Epoxyallyl Alcohols with Acids as a Tool for Ready Access to Chiral 1,2,3-Triol Monoesters: Application to Stereoselective Total Synthesis of Macrolides
  The Journal of Organic Chemistry, 2011
• First stereoselective total synthesis of decarestrictine O via RCM protocol
  Tetrahedron Letters, 2010
• Total synthesis of decarestrictine I and botryolide B via RCM protocol
  Organic & Biomolecular Chemistry, 2010
• Stereoselective First Total Synthesis of a Ten-Membered Macrolide from l-Malic Acid and (2R)-2,3-O-Cyclohexylideneglyceraldehyde
  Synlett, 2008
• Stereoselective Total Synthesis of (-)-Aspinolide B from (R)-2,3-O-Isopropylideneglyceraldehyde
  Synthesis, 2007
• Stereoselective total synthesis of (−)-decarestrictine D from l-malic acid
  Tetrahedron Letters, 2006
• Tubelactomicin A, a Novel 16-Membered Lactone Antibiotic, from Nocardia sp. I. Taxonomy, Production, Isolation and Biological Properties.
  The Journal of Antibiotics, 2000
• Epothilone A and B—Novel 16‐Membered Macrolides with Cytotoxic Activity: Isolation, Crystal Structure, and Conformation in Solution
  Angewandte Chemie International Edition, 1996