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

Authors
Jillella, RaveendraOh, Chang Ho
Issue Date
Jun-2018
Publisher
ROYAL SOC CHEMISTRY
Citation
RSC ADVANCES, v.8, no.39, pp.22122 - 22126
Indexed
SCIE
SCOPUS
Journal Title
RSC ADVANCES
Volume
8
Number
39
Start Page
22122
End Page
22126
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/149912
DOI
10.1039/c8ra03712d
ISSN
2046-2069
Abstract
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 via copper-catalyzed one-pot sequential intramolecular hydroamination (C-N bond formation) of 2-alkynylanilines followed by oxidative C-C coupling with benzoquinones.
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