Abstract
Three amino acid analogues of citric acid siderophores were synthesized. The synthetic strategy involved condensation of 2-tert-butyl-l, 3-di(N-hydroxysuccinimidyl) or 2-tert-butyl-l, 3-bis(pentachlorophenyl)citrates with N-ethyl-w-aminoalkylhydroxamates. The examination of biological properties of the obtained compounds revealed their poor, if any side-rophore activity and thus confirmed the structural requirements previously suggested for side-rophores of this type. © 1991, Walter de Gruyter. All rights reserved.
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Neilands, J. B., & Chimiak, A. (1991). Synthesis of Amino Acids Analogues of Citric Acid Siderophores. Zeitschrift Fur Naturforschung - Section B Journal of Chemical Sciences, 46(1), 117–122. https://doi.org/10.1515/znb-1991-0121
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