CoIII-Catalyzed C-H Alkenylation and Allylation with Cyclopropenes via Sequential C-H/C-C Bond Activation

被引:9
|
作者
Kim, Ye Lim [1 ]
Park, Sun-a [1 ]
Choi, Seoung-Mi [1 ]
Park, Jong-Un [1 ]
Kim, Ju Hyun [1 ]
机构
[1] Gyeongsang Natl Univ, Res Inst Nat Sci, Dept Chem BK21 FOUR, Jinju 52828, South Korea
基金
新加坡国家研究基金会;
关键词
FUNCTIONALIZATION; ACCESS; ARENES;
D O I
10.1021/acs.orglett.1c02219
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An atom-economical strategy for the C-H alkenylation and C-H allylation of arenes by employing cyclopropenes as versatile alkenylating and allylating reagents is reported, catalyzed by cobalt. The Co-catalyzed C-H alkenylation process involves sequential C-H and C-C bond cleavage. Under the optimized conditions, broad-ranging alkenylated (hetero)arenes were synthesized with complete (E)-stereoselectivity (up to 91%). The consecutive C-H allylation proved viable under basic conditions via double-bond migration of the initially generated alkenyl (hetero)arenes, thus leading to allylated (hetero)arenes with high stereoselectivity of olefin (E/Z ratio = 91:9 to 100:0).
引用
收藏
页码:6674 / 6679
页数:6
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