Chemoselective amide ligations by decarboxylative condensations of N-alkylhydroxylamines and α-ketoacids

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Abstract

(Chemical Equation Presented) Additive-free: The chemoselective amide-bond-forming ligation between N-alkylhydroxylamines and α-ketoacids requires no reagents and the only by-products are water and carbon dioxide. This process proceeds on unprotected peptide substrates without epimerization, and as such, this process has the potential to serve as a novel chemoselective ligation for the synthesis of peptides and complex materials. © 2006 Wiley-VCH Verlag GmbH & Co. KGaA.

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Bode, J. W., Fox, R. M., & Baucom, K. D. (2006). Chemoselective amide ligations by decarboxylative condensations of N-alkylhydroxylamines and α-ketoacids. Angewandte Chemie - International Edition, 45(8), 1248–1252. https://doi.org/10.1002/anie.200503991

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