Copper-Mediated Direct C2-Cyanation of Indoles Using Acetonitrile as the Cyanide Source

Cyanation Nitrogen atom
DOI: 10.1021/jo4014904 Publication Date: 2013-08-19T21:33:31Z
ABSTRACT
A copper-mediated C2-cyanation of indoles using cheap and commercially available acetonitrile as the "nonmetallic" cyanide source was achieved through sequential C-C C-H bond cleavages. The installation a removable pyrimidyl group on indole nitrogen atom is key for this C2 selectivity. This approach provides novel alternative route leading to indole-2-carbonitrile.
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