Abstract
Three amino acids were converted into the derivatives 5.2 (from glycine), 6.4a and 6.4b (from alanine), and 8.3a and 8.3b (from O-benzyl serine). These N-alkylated amino acids, which can be deprotected after conversion of the carboxyl into an amide, correspond to the general structure 2.1, a compound class of use in the study of peptide segment coupling by the ligation-acyl transfer method.
Original language | English |
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Pages (from-to) | 9247-9254 |
Number of pages | 8 |
Journal | Journal of Organic Chemistry |
Volume | 68 |
Issue number | 24 |
DOIs | |
Publication status | Published - Nov 28 2003 |
Externally published | Yes |
ASJC Scopus subject areas
- Organic Chemistry