Oxidative rearrangement of indoles to oxindoles
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2012/RA/C2RA21800C
Reference26 articles.
1. Indolocarbazole natural products: occurrence, biosynthesis, and biological activity
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3. A Novel One-Pot Approach of Hexahydropyrrolo[2,3-b]indole Nucleus by a cascade addition/cyclization strategy: Synthesis of (±)-Esermethole
4. Synthesis of β- and γ-Carbolinones via Pd-Catalyzed Direct Dehydrogenative Annulation (DDA) of Indole-carboxamides with Alkynes Using Air as the Oxidant
5. Anhydrous CeCl3 catalyzed C3-selective propargylation of indoles with tertiary alcohols
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1. The first synthesis of cis-N,N′-dialkylisoindigo derivatives from 3-indolyl-2-oxindoles with DDQ;Tetrahedron Letters;2018-03
2. Facile Synthesis of Isoindigo Derivatives from 3-Indolyl-2-Oxindoles with DDQ;Bulletin of the Korean Chemical Society;2017-11-06
3. Benzoic acid: an efficient and rapid catalyst for the synthesis of α-hydroxyl(indolyl)ethanones from indoles;Chemical Research in Chinese Universities;2016-03-19
4. The dicarbonylation of indoles via Friedel–Crafts reaction with dicarbonyl nitrile generated in situ and retro-cyanohydrination;RSC Advances;2016
5. Friedel–Crafts reaction of indoles with vicinal tricarbonyl compounds generated in situ from 1,3-dicarbonyl compounds and TEMPO: highly selective synthesis of tertiary alcohols;RSC Advances;2015
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