Synthesis of 17-membered azalides from a 16-membered macrolide utilizing amide-selective silane reduction

Synthesis of 17-membered azalides from a 16-membered macrolide utilizing amide-selective silane reduction Synthesis of 6-O-methyl-azithromycin and its ketolide analogue via Beckmann rearrangement of 9(E)-6-O-methyl-erythromycin oxime The total synthesis of hypodematine Synthesis of Dihydromotuporamine C via 3‐Azonia‐Cope Rearrangement of 11‐Membered Cyclic α‐Vinylamine The synthesis of novel 8a-aza-8a-homoerythromycin derivatives via the beckmann rearrangement of (9z)-erythromycin a oxime Novel azalides derived from 16-membered macrolides. III. Azalides modified at the C-15 and 4″ positions: Improved antibacterial activities Synthesis of Tetracyclic Core Structure of Daphnezomines A and B Synthesis and Antibacterial Activity of a Novel Class of 15-Membered Macrolide Antibiotics, “11a-Azalides” Highly Efficient and Stereoselective Mukaiyama Aldol Reaction with Chiral Aziridine‐2‐carboxaldehyde and Its Synthetic Applications Total Synthesis of Talatisamine: Exploration of Convergent Synthetic Strategies