N-Acylsaccharins as Amide-Based Arylating Reagents via Chemoselective N-C Cleavage: Pd-Catalyzed Decarbonylative Heck Reaction

被引:87
作者
Liu, Chengwei [1 ]
Meng, Guangrong [1 ]
Szostak, Michal [1 ]
机构
[1] Rutgers State Univ, Dept Chem, 73 Warren St, Newark, NJ 07102 USA
关键词
CROSS-COUPLING REACTIONS; NITROGEN BOND-CLEAVAGE; TWISTED AMIDES; AROYL CHLORIDES; ARYL BROMIDES; ACTIVATION; OLEFINATION; ALKENES; HALIDES; ESTERS;
D O I
10.1021/acs.joc.6b02294
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Palladium-catalyzed decarbonylative Heck reaction of amides by chemoselective N-C activation using N-acylsaccharins as coupling partners has been accomplished. These studies represent only the second example of amide Heck reactions reported to date. A broad range of electronically diverse amide and olefin coupling partners is amenable to this transformation. Orthogonal site-selective Heck cross couplings by C-Br/N-C cleavage and mechanistic studies are reported. This report introduces readily available, bench-stable, access versatile aryl-metal intermediates. cheap, and benign N-acylsaccharins as aryl transfer reagents to access versatile aryl-metal intermediates.
引用
收藏
页码:12023 / 12030
页数:8
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