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Nickel-Catalyzed Site-Selective Amidation of Unactivated C(sp~3)-H Bonds

机译:未活化的C(sp〜3)-H键的镍催化位点选择性酰胺化

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摘要

Intramolecular dehydrogenative cyclization of aliphatic amides was achieved on unactivated sp~3 carbon atoms by a nickel-catalyzed C-H bond functionalization process with the assistance of a bidentate directing group. The reaction favors the C-H bonds of β-methyl groups over the γ-methyl or β-methylene groups. Additionally, a predominant preference for the β-methyl C-H bonds over the aromatic sp~2 C-H bonds was observed. Moreover, this process also allows for the effective functionalization of benzylic secondary sp~3 C-H bonds.
机译:脂族酰胺的分子内脱氢环化反应是通过镍催化的C-H键官能化过程以及双齿导向基团在未活化的sp〜3碳原子上实现的。与γ-甲基或β-亚甲基相比,该反应有利于β-甲基的C-H键。另外,观察到相对于芳香族sp〜2 C-H键,β-甲基C-H键具有更大的优势。而且,该方法还允许苄基仲sp 3 C-H键的有效官能化。

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