Formation of 6,13-dimethyl-5,12-diazachrysene by oxidative coupling of 2-methylindole followed by base-induced ring-expansion
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Oxidation of methyl indole-3-acetate induced by FeCl3 and secondary amines
2. Distinguishing Features of Indolyl Radical and Radical Cation: Implications for Tryptophan Radical Studies
3. One-electron oxidation of indoles and acid-base properties of the indolyl radicals
4. Zur Chemie des Indols, V. Über die Oxydation von Indolderivaten mit Eisen (III)‐Chlorid
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1. Metal-free hydrogen transfer reduction of 3-hydroxy-3-indolyloxindoles: a novel method for the synthesis of 3,3′-biindolin-2-ones;New Journal of Chemistry;2018
2. TEMPO-catalyzed oxidative dimerization and cyanation of indoles for the synthesis of 2-(1H-indol-3-yl)-3-oxoindoline-2-carbonitriles;Tetrahedron;2017-03
3. A multifunctionalized strategy of indoles to C2-quaternary indolin-3-ones via a TEMPO/Pd-catalyzed cascade process;Organic & Biomolecular Chemistry;2017
4. TEMPO-catalyzed oxidative homocoupling route to 3,2′-biindolin-2-ones via an indolin-3-one intermediate;RSC Advances;2017
5. CU2O-Catalyzed C(SP3)-H/C(SP3)-H Cross-Coupling Using TEMPO: Synthesis of 3-(2-Oxoalkyl)-3-hydroxyoxindoles;Synthetic Communications;2015-11-11
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