Synthesis of Amino Acids Analogues of Citric Acid Siderophores

1Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

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.

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free