Rhodium(III)-Catalyzed Regioselective C3–H Acylmethylation of [2,2′-Bipyridine]-6-carboxamides with Sulfoxonium Ylides
2019
Yu, Jia | Wen, Si | Ba, Dan | Lv, Weiwei | Chen, Yanhui | Cheng, Guolin
A rhodium(III)-catalyzed C–H acylmethylation of tridentate [2,2′-bipyridine]-6-carboxamides was developed. A variety of [2,2′-bipyridine]-6-carboxamides could be monoalkylated exclusively at the C3 position with sulfoxonium ylides as carbene precursors, giving 3-alkylated products in high yields. This protocol proceeds through a rollover cyclometalation pathway, has a broad range scope of substrates, and exhibits excellent functional group tolerance.
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书目信息
出版者
American Chemical Society
其它主题
Carbon-hydrogen bond activation; Regioselectivity; Moieties; Carbenes
语言
英语
类型
Journal Article; Text
2024-02-28
MODS