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- W2037783971 endingPage "3641" @default.
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- W2037783971 abstract "A practical synthesis of the previously unreported N-acetyl-D-allosamine glycomimetic DAJNAc is described. The reaction sequence involves Pd-catalyzed allylic substitution by phthalimide in an azaheterobicyclic scaffold as the key step. The new iminosugar resulted in being a stronger β-N-acetylglucosaminidase (human placenta) competitive inhibitor than the D-gluco (DNJNAc) and D-galacto (DGJNAc) stereoisomers." @default.
- W2037783971 created "2016-06-24" @default.
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- W2037783971 date "2013-06-26" @default.
- W2037783971 modified "2023-10-16" @default.
- W2037783971 title "Stereoselective Synthesis of 2-Acetamido-1,2-dideoxyallonojirimycin (DAJNAc), a New Potent Hexosaminidase Inhibitor" @default.
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- W2037783971 doi "https://doi.org/10.1021/ol401517x" @default.
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