Direct observation of the reaction of the quinone-methide from 5,6-dihydroxyindole with the nucleophilic azide ion
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. Progress in the chemistry of melanins and related metabolites
2. One-electron oxidation of methoxylated and hydroxylated indoles by azide. 1. Characterization of the primary indolic radicals
3. Reactions of indolic radicals produced upon one-electron oxidation of 5,6-dihydroxyindole and its N(1)-methylated analogue
4. A pulse radiolysis investigation of the oxidation of indolic melanin precursors: evidence for indolequinones and subsequent intermediates
5. A pulse radiolysis investigation of the oxidation of methoxylated metabolites of indolic melanin precursors
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1. Reactivities of Quinone Methides versus o-Quinones in Catecholamine Metabolism and Eumelanin Biosynthesis;International Journal of Molecular Sciences;2016-09-20
2. Preparation of Triazoloindoles via Tandem Copper Catalysis and Their Utility as α-Imino Rhodium Carbene Precursors;Organic Letters;2014-02-11
3. Optical properties of clusters and molecules from real-time time-dependent density functional theory using a self-consistent field;Molecular Physics;2010-07-20
4. Reactivity of syringyl quinone methide intermediates in dehydrogenative polymerization I: high-yield production of synthetic lignins (DHPs) in horseradish peroxidase-catalyzed polymerization of sinapyl alcohol in the presence of nucleophilic reagents;Journal of Wood Science;2009-12-23
5. Dopaquinone redox exchange with dihydroxyindole and dihydroxyindole carboxylic acid;Pigment Cell Research;2006-10
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