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- W2950601752 abstract "A set of enantiomerically pure N-disubstituted β-amino alcohols was chlorinated by treatment with thionyl chloride. This reaction gave a mixture of regioisomeric chlorides that could be equilibrated to the more stable regioisomer by heating in DMF. The chlorides thus obtained were engaged in an intramolecular anionic ring-closure and gave access to fully protected enantio- and diastereomerically pure 2,3-cis-disubstituted azetidinic amino acids. One of the latter was deprotected and included in a short peptide sequence." @default.
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- W2950601752 date "2006-01-01" @default.
- W2950601752 modified "2023-09-26" @default.
- W2950601752 title "Stereocontrolled Synthesis of 3-Substituted Azetidinic Amino Acids" @default.
- W2950601752 doi "https://doi.org/10.1055/s-2006-933125" @default.
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