Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/60622
Title: Synthesis of n-protected peptide alcohols catalyzed by subtilisin or α-chymotrypsin in organic solvents
Authors: Liu, P
Tian, GL
Lo, WH 
Lee, KS
Ye, YH
Issue Date: 2002
Publisher: Taylor & Francis
Source: Preparative biochemistry and biotechnology, 2002, v. 32, no. 1, p. 29-37 How to cite?
Journal: Preparative biochemistry and biotechnology 
Abstract: A series of N-protected peptide alcohols were synthesized using amino alcohols with unprotected hydroxy groups as amino components by the catalysis of subtilisin or α-chymotrypsin in organic solvents. N-protected aromatic amino acid esters were more suitable as acyl donors for subtilisin. The influences of different N-protecting groups, organic solvents, and content of water on synthesis of N-protected peptide alcohols were systematically studied.
URI: http://hdl.handle.net/10397/60622
ISSN: 1082-6068 (print)
1532-2297 (online)
DOI: 10.1081/PB-120013159
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