Sustainable Ruthenium(II)-Catalyzed C-H Activations in and on H2O

被引:29
作者
Kaplaneris, Nikolaos [1 ]
Vilches-Herrera, Marcelo [1 ,2 ]
Wu, Jun [1 ]
Ackermann, Lutz [1 ,3 ]
机构
[1] Georg August Univ Gottingen, Inst Organ & Biomol Chem, Tammannstr 2, D-237077 Gottingen, Germany
[2] Univ Chile, Fac Sci, Las Palmeras 3425, Nunoa, Chile
[3] Georg August Univ Gottingen, Wohler Res Inst Sustainable Chem WISCh, Tammannstr 2, D-237077 Gottingen, Germany
基金
欧洲研究理事会;
关键词
C-H Functionalization; Ruthenium; Water; Micelles; Industry; BOND FUNCTIONALIZATION; ARYLATION REACTIONS; UNIQUE REACTIVITY; OXIDASE CATALYSIS; ORGANIC-SYNTHESIS; CARBOXYLIC-ACIDS; AROMATIC-ACIDS; ARYL CHLORIDES; WATER; ALKENYLATIONS;
D O I
10.1021/acssuschemeng.2c00873
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Catalyzed C-H activation has surfaced as an enabling tool for molecular assembly, with a plethora of translational applications. The enormous developments toward the utilization of ubiquitous C-H bonds as latent functionalities has thus enabled the efficient assembly of increasingly complex scaffolds. Recently, a paradigm shift has occurred to enable sustainable, industry-relevant C-H functionalization manifolds. Among the most prominent transition metals for C-H activations, ruthenium offers several salient features, including cost-effective, robust, and mild C-H activations with unique reactivities for remote functionalization. Indeed, ruthenium(II) catalysis by carboxylate assistance offers a highly functional group tolerant and predictable toolbox for directed as well as nondirected C-H functionalizations, with a major impact to improve the sustainability in industrial settings. These assets have allowed the use of nontoxic, nonflammable, and cost-effective H2O as a reaction medium for sustainable ruthenium(II)-catalyzed C-H activations. In this perspective, we summarize the potential of water for sustainable ruthenium(II)-catalyzed C-H activations up to February 2022.
引用
收藏
页码:6871 / 6888
页数:18
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