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

Title
Copper-catalyzed tandem reaction of 2-alkynylanilines with benzoquinones: efficient access to 3-indolylquinones
Author
오창호
Keywords
CONJUGATE ADDITION; P-QUINONES; INDOLES; 2,5-DIHYDROXY-3-(INDOL-3-YL)BENZOQUINONES; ASTERRIQUINONE; CONDENSATION; DERIVATIVES; PROTOCOL; ROUTE
Issue Date
2018-06
Publisher
ROYAL SOC CHEMISTRY
Citation
RSC ADVANCES, v. 8, no. 39, page. 22122-22126
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.
URI
https://pubs.rsc.org/en/content/articlelanding/2018/RA/C8RA03712D#!divAbstracthttps://repository.hanyang.ac.kr/handle/20.500.11754/119048
ISSN
2046-2069
DOI
10.1039/c8ra03712d
Appears in Collections:
COLLEGE OF NATURAL SCIENCES[S](자연과학대학) > CHEMISTRY(화학과) > Articles
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