ChemInform Abstract: Orthogonally Protected Schoellkopf′s Bis‐Lactim Ethers for the Asymmetric Synthesis of α‐Amino Acid Derivatives and Dipeptide Esters
摘要:
A diastereoselective trans-alkylation of aza-enolates of orthogonally protected chiral bis-lactim ethers with electrophiles, such as alkyl halides, and subsequent deprotection via hydrolysis/hydrogenation leads to dipeptide ester derivatives.
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关键词:
amino acids, peptides, proteins diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism) protection, deprotection
DOI:
10.1002/chin.201647207
年份:
2016
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