Photocatalytic Oxidative C-H Thiolation: Synthesis of Benzothiazoles and Sulfenylated Indoles

被引:15
|
作者
Dinh, Andrew N. [1 ]
Nguyen, Ashley D. [1 ]
Aceves, Ernesto Millan [1 ]
Albright, Samuel T. [1 ]
Cedano, Mario R. [1 ]
Smith, Diane K. [1 ]
Gustafson, Jeffrey L. [1 ]
机构
[1] San Diego State Univ, Dept Chem & Biochem, 5500 Campanile Dr, San Diego, CA 92182 USA
基金
美国国家科学基金会;
关键词
photoredox catalysis; benzothiazole; indole; thiolation; C-H functionalization; PHOTOREDOX CATALYSIS; BOND FORMATION; AFFINITY; ARENES;
D O I
10.1055/s-0039-1690107
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
We report studies on the photocatalytic formation of C-S bonds to form benzothiazoles via an intramolecular cyclization and sulfenylated indoles via an intermolecular reaction. Cyclic voltammetry (CV) and density functional theory studies suggest that benzothiazole formation proceeds via a mechanism that involves an electrophilic sulfur radical, while the indole sulfenylation likely proceeds via a nucleophilic sulfur radical adding into a radical cationic indole. These conditions were successfully extended to several thiobenzamides and indole substrates.
引用
收藏
页码:1648 / 1655
页数:8
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