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• W2083035513 abstract "Peptide formation on the N-terminal of 1-aminoazetidine-2-carboxylic acid is rendered problematic due to a ring opening reaction. However C-terminal development is possible and two diastereomeric mixed hydrazino dipeptides were prepared. Solution-state studies of these compounds suggest the presence of intramolecular hydrogen bonding, consistent with a hydrazino turn, and the crystal structure of one of these compounds shows a horse-shoe conformation, centered around what appears to be a hydrazino turn involving three hydrogen bond acceptors." @default.
• W2083035513 created "2016-06-24" @default.
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• W2083035513 date "2013-02-01" @default.
• W2083035513 modified "2023-09-25" @default.
• W2083035513 title "Reactivity of 1-aminoazetidine-2-carboxylic acid during peptide forming procedures: observation of an unusual variant of the hydrazino turn" @default.
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• W2083035513 doi "https://doi.org/10.1016/j.tetlet.2012.11.112" @default.
• W2083035513 hasPublicationYear "2013" @default.
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