Palladium-Catalyzed Reductive Heck Hydroarylation of Unactivated Alkenes Using Hydrosilane at Room Temperature

被引:5
|
作者
Shirai, Takahiro [1 ]
Migitera, Yusuke [2 ]
Nakajima, Ryo [1 ]
Kumamoto, Takuya [1 ]
机构
[1] Hiroshima Univ, Grad Sch Biomed & Hlth Sci, Hiroshima 7348553, Japan
[2] Hiroshima Univ, Sch Pharmaceut Sci, Hiroshima 7348553, Japan
来源
JOURNAL OF ORGANIC CHEMISTRY | 2024年 / 89卷 / 04期
关键词
ADDITION TYPE REACTION; CARBONYL-COMPOUNDS; ARYL IODIDES; ARYLATION; HYDROGEN; OLEFINS; HYDROCARBOFUNCTIONALIZATION; SUBSTITUTION; ACTIVATION; HALIDES;
D O I
10.1021/acs.joc.3c02488
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The reductive Heck hydroarylation of unactivated alkenes has emerged as an essential reaction for regioselective hydroarylation. Herein, we report a palladium-catalyzed reductive Heck hydroarylation of unactivated alkenes under mild conditions with enhanced functional group tolerance using hydrosilane as the reducing reagent. Under the optimal conditions, the alkylarene yields increased, resulting in minimal undesired products. Mechanistic studies using deuterated reagents indicated the involvement of two competing catalytic cycles.
引用
收藏
页码:2787 / 2793
页数:7
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