Department of Chemistry, Rutgers University , 73 Warren Street, Newark, New Jersey 07102, United States.
Org Lett. 2018 Jan 19;20(2):341-344. doi: 10.1021/acs.orglett.7b03567. Epub 2017 Dec 28.
The ruthenium(II)-catalyzed, heteroatom-directed C-H arylation of indoles with arylsilanes in water has been developed. The method represents the first example of a ruthenium(II)-catalyzed oxidative C-H arylation in water/aqueous media as a sustainable solvent for C-H functionalization. The reaction enables the synthesis of a wide range of indoles with exquisite selectivity for arylation at the C-2 position. Preliminary mechanistic studies indicate reversibility of the C-H ruthenation step under the developed reaction conditions.
钌(II)催化、杂原子导向的吲哚与芳基硅烷在水中的 C-H 芳基化反应已经被开发出来。该方法代表了首例钌(II)催化的在水/水介质中的氧化 C-H 芳基化反应,是 C-H 功能化的可持续溶剂。该反应能够合成广泛的吲哚类化合物,对 C-2 位的芳基化具有极好的选择性。初步的机理研究表明,在开发的反应条件下,C-H 钌化步骤具有可逆性。