Copper-catalyzed tandem reaction of 2-alkynylanilines with benzoquinones: efficient access to 3-indolylquinones

A simple, mild, catalytic and efficient method for the straightforward synthesis of an interesting class of 2-aryl/alkyl-substituted-3-indolyl quinones in good to high yields is reported for the first time. This atom-efficient method proceeds copper-catalyzed one-pot sequential intramolecular hydroa...

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Veröffentlicht in:RSC advances 2018-01, Vol.8 (39), p.22122-22126
Hauptverfasser: Jillella, Raveendra, Oh, Chang Ho
Format: Artikel
Sprache:eng
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Zusammenfassung:A simple, mild, catalytic and efficient method for the straightforward synthesis of an interesting class of 2-aryl/alkyl-substituted-3-indolyl quinones in good to high yields is reported for the first time. This atom-efficient method proceeds copper-catalyzed one-pot sequential intramolecular hydroamination (C-N bond formation) of 2-alkynylanilines followed by oxidative C-C coupling with benzoquinones.
ISSN:2046-2069
2046-2069
DOI:10.1039/c8ra03712d