Efficient and Stereoselective Synthesis of Yellow Scale Pheromone via Alkyne Haloboration, Zr-Catalyzed Asymmetric Carboalumination of Alkenes (ZACA Reaction), and Pd-Catalyzed Tandem Negishi Coupling

Ähnliche Einträge

• Fully Reagent-Controlled Asymmetric Synthesis of (−)-Spongidepsin via the Zr-Catalyzed Asymmetric Carboalumination of Alkenes (ZACA Reaction)
  von: Zhu, Gangguo, et al.
  Veröffentlicht: (2007)
• Highly enantioselective synthesis of γ-, δ-, and ε-chiral 1-alkanols via Zr-catalyzed asymmetric carboalumination of alkenes (ZACA)–Cu- or Pd-catalyzed cross-coupling
  von: Xu, Shiqing, et al.
  Veröffentlicht: (2014)
• Highly Regio- and Stereoselective Synthesis of (Z)-Trisubstituted Alkenes via Propyne Bromoboration and Tandem Pd-Catalyzed Cross-Coupling
  von: Wang, Chao, et al.
  Veröffentlicht: (2009)
• Alkyne Elementometalation–Pd-Catalyzed Cross-Coupling. Towards Synthesis of Various Types of Acyclic Alkenes in High Yields, Efficiently, Selectively, Economically, and Safely—“Green” Way
  von: Negishi, Ei-ichi, et al.
  Veröffentlicht: (2010)
• Arylethyne Bromoboration–Negishi Coupling Route to E- or Z-Aryl-Substituted Trisubstituted Alkenes of ≥98% IsomericPurity. New Horizon in the Highly Selective Synthesis of Trisubstituted Alkenes
  von: Wang, Chao, et al.
  Veröffentlicht: (2010)