PubMed · 9023966
A reductive acidolysis final deprotection strategy in solid phase peptide synthesis based on safety-catch protection.
Abstract
A reductive acidolysis final deprotection strategy in solid phase peptide synthesis was developed using a new safety-catch type of semi-permanent protecting groups and new linkers which were derived from 4-methylsulfinylbenzyl protection. This new strategy was based on a two-dimensional protection scheme employing acid-labile temporary and acid-stable but reductive acidolysis-cleavable semi-permanent protecting groups. By using this strategy, we successfully synthesized four model peptides, of which two contained C-terminal amide.
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T Kimura, T Fukui, S Tanaka, K Akaji, Y Kiso. 1997. A reductive acidolysis final deprotection strategy in solid phase peptide synthesis based on safety-catch protection.. https://doi.org/10.1248/cpb.45.18
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