Copper-catalyzed cyanation of arenes using benzyl nitrile as a cyanide anion surrogate
2012; Royal Society of Chemistry; Volume: 48; Issue: 79 Linguagem: Inglês
10.1039/c2cc35046g
ISSN1364-548X
AutoresJisong Jin, Qiaodong Wen, Ping Lü, Yanguang Wang,
Tópico(s)Oxidative Organic Chemistry Reactions
ResumoThe copper-catalyzed cyanation of arenes using benzyl nitrile as a cyanide anion surrogate furnishes aromatic nitriles in moderate to good yields. The cascade process involves a copper-catalyzed aerobic C–H oxidation, a retro-cyanohydrination, and a copper-catalyzed aerobic oxidative C–H functionalization.
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