Cobalt-Catalyzed C-H Cyanation of (Hetero)arenes and 6-Arylpurines with N-Cyanosuccinimide as a New Cyanating Agent

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A cobalt-catalyzed C-H cyanation reaction of arenes has been developed using N-cyanosuccinimide as a new electrophilic cyanating agent. The reaction proceeds with high selectivity to afford monocyanated products with excellent functional group tolerance. Substrate scope was found to be broad enough to include a wide range of heterocycles including 6-arylpurines.
Publisher
AMER CHEMICAL SOC
Issue Date
2015-02
Language
English
Article Type
Article
Keywords

PHENYL-P-TOLUENESULFONAMIDE; BOND ACTIVATION; AMMONIUM IODIDE; CYTOSTATIC ACTIVITY; CYANIDE SOURCE; ARYL; FUNCTIONALIZATION; NUCLEOSIDES; INDOLES; DERIVATIVES

Citation

ORGANIC LETTERS, v.17, no.3, pp.660 - 663

ISSN
1523-7060
DOI
10.1021/ol503680d
URI
http://hdl.handle.net/10203/195824
Appears in Collection
CH-Journal Papers(저널논문)
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