Non-Heme-Type Ruthenium Catalyzed Chemo- and Site-Selective C-H Oxidation

被引：21

作者：

Doiuchi, Daiki ^{[2
]}

Nakamura, Tatsuya ^{[2
]}

Hayashi, Hiroki ^{[1
]}

Uchida, Tatsuya ^{[1
,3
]}

机构：

[1] Kyushu Univ, Fac Arts & Sci, Nishi Ku, 744 Motooka, Fukuoka 8190395, Japan

[2] Kyushu Univ, Grad Sch Sci, Dept Chem, Nishi Ku, 744 Motooka, Fukuoka 8190395, Japan

[3] Kyushu Univ, Int Inst Carbon Neutral Energy Res WPI 12CNER, Nishi Ku, 744 Motooka, Fukuoka 8190395, Japan

来源：

CHEMISTRY-AN ASIAN JOURNAL | 2020年 / 15卷 / 06期

关键词：

C-H oxidation; Non-Heme model; Hydroxylation; Ruthenium; Site-selective oxidation; NONHEME IRON CATALYSTS; BOND OXIDATION; ALKANE HYDROXYLATION; ATOM ECONOMY; COMPLEXES; OXYGENATION; REACTIVITY; FUNCTIONALIZATION; ACTIVATION; MECHANISM;

D O I：

10.1002/asia.202000134

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Herein, we developed a Ru(II)(BPGA) complex that could be used to catalyze chemo- and site-selective C-H oxidation. The described ruthenium complex was designed by replacing one pyridyl group on tris(2-pyridylmethyl)amine with an electron-donating amide ligand that was critical for promoting this type of reaction. More importantly, higher reactivities and better chemo-, and site-selectivities were observed for reactions using the cis-ruthenium complex rather than the trans-one. This reaction could be used to convert sterically less hindered methyne and/or methylene C-H bonds of a various organic substrates, including natural products, into valuable alcohol or ketone products.

引用

页码：762 / 765

页数：4

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