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- W2331857761 abstract "Copper(I)-catalyzed cycloaddition of synthetic and bacterial copolyesters bearing pendant alkyne group with mono-(6-azido-6-desoxy)-β-cyclodextrin was carried out to synthesize β-CD-functionalized copolyester. The synthetic “clickable” copolyesters were obtained by the ring-opening copolymerization of the propargyl-modified lactones and ε-caprolactone. The bacterial copolyesters containing an alkyne group were biosynthesized from a mixture of 10-undecynoic acid and hexanoic acid by the Gram-negative bacteria Pseudomonas oleovorans. The modified products of the “click” reaction were characterized by FT-IR, 1H NMR spectroscopy, and DSC. Furthermore, the host guest capability of covalently attached β-cyclodextrin moieties was proved by dynamic light scattering measurements." @default.
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- W2331857761 date "2011-02-21" @default.
- W2331857761 modified "2023-10-11" @default.
- W2331857761 title "Cyclodextrin-Modified Polyesters from Lactones and from Bacteria: An Approach to New Drug Carrier Systems" @default.
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- W2331857761 doi "https://doi.org/10.1021/ma1027627" @default.
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