Synthesis of novel functionalized cispentacins through C–C oxidative cleavage of diendo-norbornene beta-amino acid

Hasonló tételek

• A new access route to functionalized cispentacins from norbornene beta-amino acids
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  Megjelent: (2013)
• A stereocontrolled access to functionalized cispentacins and acyclic β2,3-amino acids through oxidative ring cleavage
  Szerző: Cherepanova Maria
  Megjelent: (2014)
• Stereocontrolled One-Step Synthesis of Difunctionalised Cispentacin Derivatives through Ring-Opening Metathesis of Norbornene β-Amino Acids
  Szerző: Kiss Loránd, et al.
  Megjelent: (2015)
• Synthesis of Highly Functionalized Fluorinated Cispentacin Derivatives
  Szerző: Nonn Melinda, et al.
  Megjelent: (2012)
• Synthesis of densely functionalized cispentacin derivatives through selective aziridination and aziridine opening reactions orthogonally protected di- and triaminocyclopentanecarboxylates /
  Szerző: Nonn Melinda, et al.
  Megjelent: (2014)