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New sulfoquinovose analogues of phosphatidylinositol 3‐phosphate have been synthesised based on a sulfoquinovose scaffold as potential protein kinase B (PKB) inhibitors. The synthetic strategy involved the introduction into glucose of a thioacetate group at the 6‐position and of an azide group at the anomeric position as precursors of the sulfonate and phosphoramidate moieties present in the final...
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