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Peptide Syntheses with the N ‐PChd Protective Group Synthesis of the Hydrophobic Segment 14–20 L‐Ala‐Leu‐Ile‐Leu‐Leu‐Ala‐Gln of Human Lymphoblastoid Interferon
Author(s) -
Khalifa Mohamed Hassen,
Jung Günther,
Rieker Anton
Publication year - 1982
Publication title -
liebigs annalen der chemie
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 0170-2041
DOI - 10.1002/jlac.198219820608
Subject(s) - chemistry , amino acid , racemization , hydrolysis , dichloromethane , peptide , yield (engineering) , peptide synthesis , organic chemistry , biochemistry , materials science , solvent , metallurgy
Amino acid esters were transformed in 59–97% yields into N ‐(3,5‐di‐ tert ‐butyl‐4‐oxo‐1‐phenyl‐2,5‐cyclohexadienyl)amino acid esters ( N ‐PChd amino acid esters) 8 via anodic oxidation in the presence of 2,6‐di‐ tert ‐butyl‐4‐phenylphenol ( 1a ). Hydrolysis of 8 lead to the corresponding N ‐PChd amino acids 9 . The novel PChd protective group is stable towards basic reagents, it can be removed by hydrogenation or acidolysis, and it exhibits good solubilizing properties for oligopeptides in organic solvents. N ‐PChd amino acids couple without racemization, they are easily prepared and storable, and crystallize readily. — Using conventional methods of peptide synthesis and PChd deprotection with 10–50% trifluoroacctic acid in dichloromethane or catalytic hydrogenation, the heptapeptide HuIFN‐α(Ly)14–20 L‐Ala‐Leu‐Ile‐Leu‐Leu‐Ala‐Gln was synthesized in good yield and purity as shown by column and thin layer chromatography, 13 C‐NMR spectroscopy, chiral phase gas chromatography, and common analytical methods.