4.4 Article

Oxidation of the neurotoxin 6-nitrodopamine and related 4-nitrocatechols under biomimetic conditions

Journal

TETRAHEDRON
Volume 56, Issue 32, Pages 5941-5945

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0040-4020(00)00483-X

Keywords

coupling reactions; nitro compounds; dimerisation; biomimetic reactions

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Oxidation of 6-nitrodopamine (1) with horseradish peroxidase (HRP)/H2O2 in 0.05 M phosphate buffer, pH 7.4 afforded as main product the novel 5-[4-(2-aminoethyl)-2-hydroxy-5-nitrophenoxy]-6,7-dihydroxy-4-nitro-2,3-dihydroindole (4). Similar oxidation of the 4-nitrocatechols 2 and 3 with HRP/H2O2 or K3Fe(CN)(6) gave chiefly the dimers 5/6 and 7/8. These products arise probably via 4-nitro-o-quinone or 4-nitro-2,3-dihydroindole-6,7-dione intermediates which are trapped by the starting nitrocatechols. (C) 2000 Elsevier Science Ltd. All rights reserved.

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