Thallium(III) acetate-mediated 3,3-couplings of indoles with the formation of indolocarbazoles
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Syntheses of 6-substituted indolo[3,2-b]carbazoles, including 6-formylindolo[3,2-b]carbazole, an extremely efficient ligand for the TCDD (Ah) receptor
2. Syntheses of 6,12-disubstituted 5,11-dihydroindolo[3,2-b]carbazoles, including 5,11-dihydroindolo[3,2-b]carbazole-6,12-dicarbaldehyde, an extremely efficient ligand for the TCDD (Ah) receptor
3. Synthesis of 6-formylindolo[3,2-b]carbazole, an extremely potent ligand for the aryl hydrogen (Ah) receptor
4. Formation of 6,13-dimethyl-5,12-diazachrysene by oxidative coupling of 2-methylindole followed by base-induced ring-expansion
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1. Stereospecific Approach to the Synthesis of Ring-A Oxygenated Sarpagine Indole Alkaloids. Total Synthesis of the Dimeric Indole Alkaloid P-(+)-Dispegatrine and Six Other Monomeric Indole Alkaloids;The Journal of Organic Chemistry;2013-06-18
2. Metal-free Catalyzed Oxidative Trimerization of Indoles by Using TEMPO in Air: An Entry into 3-(1H-indol-3-yl)-3,3'-biindolin-2-ones;Current Organic Synthesis;2013-05-01
3. Photophysical properties of indolo[3,2-b]carbazoles as a promising class of optoelectronic materials;Semiconductors;2010-12
4. ChemInform Abstract: Thallium(III) Acetate Mediated 3,3-Couplings of Indoles with the Formation of Indolocarbazoles.;ChemInform;2010-06-11
5. Thallium(III) in Organic Synthesis;Synthesis;2010-02-08
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