Exploration of the four-dimensional-conformational potential energy hypersurface of N-acetyl-L-aspartic acid N'-methylamide with its internally hydrogen bonded side-chain orientation

Hasonló tételek

• N-acetyl-l-aspartic acid-N'-methylamide with side-chain orientation capable of external hydrogen bonding
  Szerző: Koo J. C. P., et al.
  Megjelent: (2002)
• Conformational dependence of the intrinsic acidity of the aspartic acid residue sidechain in N-acetyl-L-aspartic acid-N '-methylamide
  Szerző: Koo Joseph C.P, et al.
  Megjelent: (2003)
• Conformational dependence of the intrinsic acidity of the aspartic acid residue sidechain in N-acetyl-L-aspartic acid-N`-methylamide
  Szerző: Koo Joseph C. P.
  Megjelent: (2003)
• Enthalpy Differences of the n-Pentane Conformers
  Szerző: Csontos József, et al.
  Megjelent: (2016)
• How reliable could economic Hartree-Fock computations be in studying large, folded peptides? A comparative HF and DFT case study on N- and C-protected aspartic acid
  Szerző: Koo JCP, et al.
  Megjelent: (2002)