Rh(III)-catalyzed direct C-H/C-H cross-coupling of quinones with arenes assisted by a directing group: identification of carbazole quinones as GSK beta inhibitors

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Rh-catalyzed direct C-H/C-H cross-coupling reaction of various (hetero)arenes with quinones is developed. This protocol is effective for a broad range of both quinone and arene substrates and a wide range of directing groups for this reaction, affording structurally diverse aryl-substituted quinones with high synthetic utility. Moreover, the present synthetic route allowed for the rapid construction of the carbazole quinone moiety that was identified as a new inhibitor scaffold for GSK beta.
Publisher
ROYAL SOC CHEMISTRY
Issue Date
2015-02
Language
English
Article Type
Article
Keywords

LATE-STAGE DIVERSIFICATION; BOND ACTIVATION; ARYLBORONIC ACIDS; DIRECT ARYLATION; FUNCTIONALIZATION; BENZOQUINONE; CONSTRUCTION; DERIVATIVES; KINASE; ROUTE

Citation

ORGANIC & BIOMOLECULAR CHEMISTRY, v.13, no.13, pp.3918 - 3923

ISSN
1477-0520
DOI
10.1039/c4ob02624a
URI
http://hdl.handle.net/10203/198324
Appears in Collection
CH-Journal Papers(저널논문)
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