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电荷转移配合物促进镍催化羰基化反应中的 C-N 键活化。

Charge-Transfer Complex Promoted C-N Bond Activation for Ni-Catalyzed Carbonylation.

机构信息

State Key Laboratory for Oxo Synthesis and Selective Oxidation, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences , Lanzhou 730000, P. R. China.

University of Chinese Academy of Sciences , Beijing 100049, P. R. China.

出版信息

Org Lett. 2017 Jul 7;19(13):3520-3523. doi: 10.1021/acs.orglett.7b01488. Epub 2017 Jun 9.

Abstract

A new strategy was developed for activation of C-N bond via formation of an amine-I charge-transfer complex, which facilitates the inert C-N bond activation via oxidative addition with Ni(0). This strategy has been successfully applied in the Ni-catalyzed carbonylation of benzylamines via direct insertion of CO into the C-N bond, which provided a straightforward and rapid approach to arylacetamides in the presence of catalytic amounts of I and Ni catalyst. Mechanistic studies suggested that a benzyl radical generated via the oxidative addition was involved in the present reaction.

摘要

开发了一种通过形成胺-I 电荷转移配合物来激活 C-N 键的新策略,该策略通过 Ni(0) 的氧化加成促进了惰性 C-N 键的活化。该策略已成功应用于 Ni 催化的苄胺羰基化反应中,通过 CO 直接插入 C-N 键,在催化量的 I 和 Ni 催化剂存在下,为芳基乙酰胺提供了一种直接快速的方法。机理研究表明,通过氧化加成生成的苄基自由基参与了本反应。

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