Abstract
We successfully prepared boroxazolidones by the reaction of diarylborinic acids substituted with electron-withdrawing groups and α-amino acids with various substituents under physiological conditions. β-Amino acids and the bioactive compound biocytin also formed related chelate compounds in good yields. Since the reaction proceeded smoothly under moderate conditions in the presence of other functional groups, it could be a powerful tool for the target identification of bioactive molecules.
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