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Org Biomol Chem ; 19(20): 4593-4598, 2021 05 26.
Article in English | MEDLINE | ID: mdl-33961001

ABSTRACT

The copper-catalyzed cycloamination of indolylquinones and various (hetero)aromatic amines under ligand-free conditions for the synthesis of polycyclic N-heterocycles has been developed. This method allows facile access to polycyclic N-heterocycles with the tolerance of chloride, bromide, amino, thio, etc. groups in moderate to high yields (60-89%).

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