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- W2949418087 abstract "Abstract The stereoselective synthesis of α-cinnamyl γ-amino acids and the corresponding oligopeptides is described. Detailed 1D and 2D NMR studies in pyridine-d 5 show that the ( αR )-cinnamyl γ-amino acid tetrapeptide adopts a reverse turn structure, while the ( αS )-cinnamyl γ-amino acid tetrapeptide adopts a right-handed helical structure." @default.
- W2949418087 created "2019-06-27" @default.
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- W2949418087 date "2010-06-13" @default.
- W2949418087 modified "2023-10-01" @default.
- W2949418087 title "ChemInform Abstract: Synthesis and Folding Preferences of γ-Amino Acid Oligopeptides: Stereochemical Control in the Formation of a Reverse Turn and a Helix." @default.
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- W2949418087 doi "https://doi.org/10.1002/chin.199935231" @default.
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