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Conference publicationsComparative conformational analysis of isolated rotamers in methylamides of N-acetyl-α-l-amino acidsRussia, Pushchino General structural and thermodynamic features of low-energy conformers in monopeptides of l-amino acids were revealed by using semi-empirical quantum-chemical calculations. We concluded, that primary realization by peptide conformers both helix-like and β-like forms is the internal property of a monopeptide molecular core itself. |
