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- W1585189007 abstract "To date, cyclo-β-tripeptides (twelve-membered-ring trilactams, C) have resisted structural investigations because of their extreme insolubility. Modelling and comparison with the corresponding tetramers indicate that the rings stack to form tube-like hydrogen-bonded aggregates (D). By exploiting the solubilizing effect of LiCl on peptides in THF, we were able to prepare the water-soluble title compound and determine its structure (E) by NMR spectroscopy. Structural similarities and differences between the trilactam ring of [β3-HGlu]3 and the corresponding trilactone ring, such as that of enterobactin (A), are discussed, and structures (`elongated'; F, G) are proposed that should be able to serve as tridentate or trivalent ligands for metal centers." @default.
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- W1585189007 date "1999-06-09" @default.
- W1585189007 modified "2023-10-16" @default.
- W1585189007 title "Preparation and NMR Structure of the Cyclo-β-tripeptide [β3-HGlu]3 in Aqueous Solution: A New Class of Enterobactin-TypeC3-Symmetrical Ligands?, Preliminary Communication" @default.
- W1585189007 doi "https://doi.org/10.1002/(sici)1522-2675(19990609)82:6<957::aid-hlca957>3.0.co;2-h" @default.
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