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• W2140403967 endingPage "223" @default.
• W2140403967 startingPage "218" @default.
• W2140403967 abstract "O-Acyl isopeptides, in which the N-acyl linkage on the hydroxyamino acid residue (e.g., Ser and Thr) is replaced with an O-acyl linkage, generally possess superior water-solubility to their corresponding native peptides, as well as other distinct physicochemical properties. In addition, O-acyl isopeptides can be rapidly converted into their corresponding native peptide under neutral aqueous conditions through an O-to-N acyl migration. By exploiting these characteristics, researchers have applied the O-acyl isopeptide method to various peptide-synthesis fields, such as the synthesis of aggregative peptides and convergent peptide synthesis. This O-acyl-isopeptide approach also serves as a means to control the biological function of the peptide in question. Herein, we report the synthesis of O-acyl isopeptides and some of their applications." @default.
• W2140403967 created "2016-06-24" @default.
• W2140403967 creator A5006557735 @default.
• W2140403967 creator A5020861873 @default.
• W2140403967 date "2013-03-20" @default.
• W2140403967 modified "2023-10-16" @default.
• W2140403967 title "Synthesis of<i>O</i>-Acyl Isopeptides" @default.
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• W2140403967 doi "https://doi.org/10.1002/tcr.201200023" @default.
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