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Title: Regioselective synthesis of 3,4,5-trisubstituted 2-aminofurans. Author: Huynh TN, Retailleau P, Denhez C, Nguyen KP, Guillaume D. Journal: Org Biomol Chem; 2014 Jul 28; 12(28):5098-101. PubMed ID: 24931912. Abstract: Three series of methyl 5-substituted 2-aminofuran-4-keto-3-carboxylates have been prepared following a multicomponent reaction strategy by the addition of an isocyanide to 4-oxo-2-butynoate in the presence of an aldehyde. The cycloaddition regioselectivity is generally high (>95%) but decreases when an electron-rich substituent is located at the butynoate 4-position.[Abstract] [Full Text] [Related] [New Search]