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- W3087703312 endingPage "7501" @default.
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- W3087703312 abstract "Oligomers of 5-amino-N-acylanthranilic acid, previously unknown aromatic oligoamides that cannot be obtained with known amide coupling methods, are synthesized based on a new, highly efficient amide-bond formation strategy that takes advantage of the ring-opening of benzoxazinone derivatives. These oligoamides offer multiple backbone NH groups as H-bond donors which, in the presence of iodide or chloride ion, are convergently arranged and H-bonded, which enforces a folded, crescent conformation. These aromatic oligoamides provide a versatile platform based on which anion-dependent foldamers, or anion binders with tunable affinity and specificity, are being constructed." @default.
- W3087703312 created "2020-09-25" @default.
- W3087703312 creator A5008313987 @default.
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- W3087703312 creator A5048618133 @default.
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- W3087703312 date "2020-09-22" @default.
- W3087703312 modified "2023-10-11" @default.
- W3087703312 title "Oligo(5-amino-<i>N</i>-acylanthranilic acids): Amide Bond Formation without Coupling Reagent and Folding upon Binding Anions" @default.
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- W3087703312 doi "https://doi.org/10.1021/acs.orglett.0c02696" @default.
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