Protonation and ring closure of stereoisomeric α-substituted cinnamic acids in superacidic media studied by 13C NMR spectroscopy and computations 1

Hasonló tételek

• Hydrogen bonding interactions in α-substituted cinnamic acid ester derivatives studied by FT–IR spectroscopy and calculations
  Szerző: Kiss T. János, et al.
  Megjelent: (2000)
• Conformational properties of a pyridyl-substituted cinnamic acid studied by NMR measurements and computations
  Szerző: Csankó Krisztián, et al.
  Megjelent: (2013)
• Modeling hydrogen bonding interactions in α-substituted cinnamic acid ester derivatives by semiempirical quantum chemical calculations
  Szerző: Körtvélyesi Tamás, et al.
  Megjelent: (2000)
• Structure Elucidation of Natural Diterpenes by NMR Spectroscopy
  Szerző: Evanics Ferenc
  Megjelent: (2005)
• C-H...F hydrogen bonds as the organising force in F-substituted alpha-phenyl cinnamic acid aggregates studied by the combination of FTIR spectroscopy and computations
  Szerző: Tolnai Balázs, et al.
  Megjelent: (2009)