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- W3023507415 endingPage "108027" @default.
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- W3023507415 abstract "Abstract A short synthetic route to a small library of aminocyclitols 14·HCl-19·HCl has been elaborated from the common shikimic acid-derived scaffolds 20 and 21. The developed strategy features three oxidative processes ‒ ozonolysis, dihydroxylation and epoxidation ‒ as the key transformations. The stereochemistry of the newly created stereocentres was confirmed either via crystallographic analysis or by means of NOESY experiments conducted on advanced intermediates. Glycosidase inhibition study revealed no glucosidase inhibition and only weak inhibitory activity against recombinant Drosophila melanogaster Golgi mannosidase (GMIIb)." @default.
- W3023507415 created "2020-05-13" @default.
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- W3023507415 date "2020-07-01" @default.
- W3023507415 modified "2023-09-24" @default.
- W3023507415 title "Synthesis and mannosidase inhibitory profile of a small library of aminocyclitols from shikimic acid-derived scaffolds" @default.
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- W3023507415 doi "https://doi.org/10.1016/j.carres.2020.108027" @default.
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