Synthesis of macrocyclic natural products by catalyst-controlled stereoselective ring-closing metathesis

Antzeko izenburuak

• Efficient and Selective Formation of Macrocyclic Disubstituted Z Alkenes by Ring-Closing Metathesis (RCM) Reactions Catalyzed by Mo- or W-Based Monoaryloxide Pyrrolide (MAP) Complexes. Applications to Total Syntheses of Epilachnene, Yuzu Lactone, Ambrettolide, Epothilone C and Nakadomarin A
  nork: Wang, Chenbo, et al.
  Argitaratua: (2013)
• Mo-Based Complexes with Two Aryloxides and a Pentafluoroimido Ligand: Catalysts for EfficientZ-Selective Synthesis of a Macrocyclic Trisubstituted Alkene by Ring-Closing Metathesis
  nork: Wang, Chenbo, et al.
  Argitaratua: (2013)
• Preparation of Macrocyclic Z-Enoates and (E,Z)- or (Z,E)-Dienoates through Catalytic Stereoselective Ring-Closing Metathesis
  nork: Zhang, Hanmo, et al.
  Argitaratua: (2014)
• Kinetically E-Selective Macrocyclic Ring-Closing Metathesis
  nork: Shen, Xiao, et al.
  Argitaratua: (2017)
• Catalyst-Controlled Stereoselective Olefin Metathesis as a Principal Strategy in Multi-Step Synthesis Design. A Concise Route to (+)-Neopeltolide()
  nork: Yu, Miao, et al.
  Argitaratua: (2014)