Ir(iii)-catalyzed ortho C-H alkylations of (hetero)aromatic aldehydes using alkyl boron reagents

被引:29
作者
Chen, Xiao-Yang [1 ]
Sorensen, Erik J. [1 ]
机构
[1] Princeton Univ, Dept Chem, Frick Chem Lab, Princeton, NJ 08544 USA
基金
美国国家科学基金会;
关键词
PALLADIUM-CATALYZED ALKYLATION; TRANSIENT DIRECTING GROUP; METHYLENE C(SP(3))-H BONDS; AROMATIC KETONES; RUTHENIUM CATALYST; ALKYLBORONIC ACIDS; SIMPLE OLEFINS; ARYLATION; BENZALDEHYDES; LIGAND;
D O I
10.1039/c8sc03606c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transition-metal-catalyzed C-H alkylation reactions directed by aldehydes or ketones have been largely restricted to electronically activated alkenes. Herein, we report a general protocol for the Ir(iii)-catalyzed ortho C-H alkylations of (hetero)aromatic aldehydes using alkyl boron reagents as the coupling partner. Featuring aniline as an inexpensive catalytic ligand, the method was compatible with a wide variety of benzaldehydes, heterocyclic aldehydes, potassium alkyltrifluoroborates as well as a few ,-unsaturated aldehydes. An X-ray crystal structure of a benzaldehyde ortho C-H iridation intermediate was also successfully obtained.
引用
收藏
页码:8951 / 8956
页数:6
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