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KAHA Ligation information


The α-Ketoacid-Hydroxylamine (KAHA) Amide-Forming Ligation is a chemical reaction that is used to join two unprotected fragments in peptide synthesis.[1][2] It is an alternative to the Native Chemical Ligation (NCL). KAHA Ligation was developed by Jeffrey W. Bode group at ETH Zürich (previously University of Pennsylvania).

  1. ^ Bode, Jeffrey W.; Fox, Ryan M.; Baucom, Kyle D. (2006). "Chemoselective Amide Ligations by Decarboxylative Condensations ofN-Alkylhydroxylamines and α-Ketoacids". Angewandte Chemie. 118 (8): 1270–1274. doi:10.1002/ange.200503991. ISSN 0044-8249.
  2. ^ Pusterla, Ivano; Bode, Jeffrey W. (2012). "The Mechanism of the α-Ketoacid-Hydroxylamine Amide-Forming Ligation". Angewandte Chemie. 124 (2): 528–531. doi:10.1002/ange.201107198. ISSN 0044-8249.

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KAHA Ligation

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The α-Ketoacid-Hydroxylamine (KAHA) Amide-Forming Ligation is a chemical reaction that is used to join two unprotected fragments in peptide synthesis....

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Ligation

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brackets KAHA Ligation Ligation-independent cloning Typographic ligature forming This disambiguation page lists articles associated with the title Ligation. If...

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Native chemical ligation

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Native Chemical Ligation (NCL) is an important extension of the chemical ligation concept for constructing a larger polypeptide chain by the covalent...

Word Count : 1384

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