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- W2022130139 endingPage "4080" @default.
- W2022130139 startingPage "4072" @default.
- W2022130139 abstract "Efficient routes for the syntheses of optically pure and hitherto unknown l-chiro- and d-allo-inositol derivatives, azido- and aminocyclitols of l-chiro-configuration, diazido- and diaminocyclitols of d-allo-configuration from economically viable myo-inositol are described. These routes provide access to synthetically flexible 1,2:4,5-di-O-isopropylidene-chiro-inositol and 1,6:3,4-di-O-isopropylidene-allo-inositol, which are otherwise difficult to synthesize directly from their parent inositols. A one pot methodology that allows rapid access to both chiro- and allo-inositol derivatives has also been developed. Investigations on the glycosidase inhibitory properties of these novel azido- and amino-inositols unraveled the potentials of these classes of compounds as novel class of glycosidase inhibitors. Both d and l forms of these cyclitols could be synthesized from myo-inositol in gram scales and hence by exploiting the difference in reactivities of cis- and trans-ketals, a variety of protected derivatives, which are useful for the synthesis of unnatural phosphoinositols and natural products, can be synthesized." @default.
- W2022130139 created "2016-06-24" @default.
- W2022130139 creator A5026200005 @default.
- W2022130139 creator A5056908243 @default.
- W2022130139 creator A5073573273 @default.
- W2022130139 creator A5078914737 @default.
- W2022130139 date "2008-04-01" @default.
- W2022130139 modified "2023-09-23" @default.
- W2022130139 title "Efficient syntheses of optically pure chiro- and allo-inositol derivatives, azidocyclitols and aminocyclitols from myo-inositol" @default.
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- W2022130139 doi "https://doi.org/10.1016/j.tet.2008.02.032" @default.
- W2022130139 hasPublicationYear "2008" @default.