Journal
AUSTRALIAN JOURNAL OF CHEMISTRY
Volume 53, Issue 5, Pages 425-433Publisher
C S I R O PUBLISHING
DOI: 10.1071/CH99082
Keywords
oxazolidinones; N-methyl amino acids; synthesis; reductive cleavage
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A range of oxazolidinones derived from N-carbamoyl alpha-amino acids were prepared by an efficient method as key intermediates in the synthesis of N-methyl amino acids and peptides. The method was readily applied to most alpha-amino acids except those with basic side chains. The oxazolidinones were converted by reductive cleavage into N-methyl alpha-amino acids.
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