A total synthesis of milbemycin G: Approaches to the C(1)-C(10)-fragment and completion of the synthesis

Chemistry

• Milbemycin 100%
• Chemical Reaction Product 66%
• Synthesis (Chemical) 66%
• Acid 66%
• Ester 66%
• Scanning Electron Microscopy 50%
• Mixture 50%
• Methylation 50%
• Trichloroacetate 50%
• Hydroxyl Group 50%
• Butenolide 50%
• Sample 33%
• Group 33%
• Reduction 33%
• Cyclization Reaction 33%
• Total Synthesis 33%
• Amount 33%
• Compound Isomer 33%
• Esterification 33%
• Ethanolysis 33%
• Oxidation Reaction 16%
• Chloride 16%
• Alkene 16%
• Dioxygen 16%
• Salt 16%
• Iodine 16%
• Enantiomer 16%
• Macrolide Antibiotic Agent 16%
• Ether 16%
• Double Bond 16%
• Tert-Butyl Hydroperoxide 16%
• Phosphonium 16%
• Isomerization 16%
• Selenide 16%
• Diketone 16%
• Oxidative Elimination Reaction 16%
• Ethyl Ester 16%
• Wittig Reaction 16%
• Saponification 16%
• Trichloroacetic Acid 16%
• Yamaguchi Esterification 16%
• (S)-Mandelate 16%