Anti-Markovnikov Hydroheteroarylation of Unactivated Alkenes with Indoles, Pyrroles, Benzofurans, and Furans Catalyzed by a Nickel鈥?i>N-Heterocyclic Carbene System

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• 作者：York Schramm ; Makoto Takeuchi ; Kazuhiko Semba ; Yoshiaki Nakao ; John F. Hartwig
• 刊名：Journal of the American Chemical Society
• 出版年：2015
• 出版时间：September 30, 2015
• 年：2015
• 卷：137
• 期：38
• 页码：12215-12218
• 全文大小：372K
• ISSN：1520-5126

文摘

We report the catalytic addition of C鈥揌 bonds at the C2 position of heteroarenes, including pyrroles, indoles, benzofurans, and furans, to unactivated terminal and internal alkenes. The reaction is catalyzed by a combination of Ni(COD)₂ and a sterically hindered, electron-rich N-heterocyclic carbene ligand or its analogous Ni(NHC)(arene) complex. The reaction is highly selective for anti-Markovnikov addition to 伪-olefins, as well as for the formation of linear alkylheteroarenes from internal alkenes. The reaction occurs with substrates containing ketones, esters, amides, boronate esters, silyl ethers, sulfonamides, acetals, and free amines.