Syntheses of alpha- and beta-C-glucopyranosyl serines from a common intermediate
Ernest G Nolen1, Laurence A Donahue, Rebecca Greaves
1Department of Chemistry, Colgate University, 13 Oak Drive, Hamilton, New York 13346, USA. enolen@colgate.edu
Abstract:
A versatile synthesis leading to either C-linked alpha- or beta-glucopyranosyl serines is presented from a common, advanced synthetic intermediate. Cyclization of the penultimate carbinol onto the alkene and methanolysis of the lactone yields selectively the alpha-linkage. A transposition of these last steps leads to the beta-linked isomer selectively.
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