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- W2017223839 abstract "Abstract An efficient and stereospecific synthesis of chiral 3,5-diaminoazepan-2-one as a novel conformationally restricted surrogate of 2,4-diaminobutanoyl (Dab)-Gly dipeptide has been achieved by an intramolecular transamidation with a catalytic hydrogenation as the key steps, starting from commercially available trans-4-hydroxy- l -proline. This methodology represents a powerful tool for the synthesis of the Dab-Gly dipeptide surrogate as one type of Freidinger e-lactam." @default.
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- W2017223839 date "2005-06-01" @default.
- W2017223839 modified "2023-09-27" @default.
- W2017223839 title "Synthesis of (3S,5R)-3,5-diaminoazepan-2-one as a conformationally restricted surrogate of the Dab-Gly dipeptide" @default.
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- W2017223839 doi "https://doi.org/10.1016/j.tetasy.2005.04.017" @default.
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