Gold-catalyzed C-H Functionalization of Phenothiazines with Aryldiazoacetates

被引:18
作者
Jana, Sripati [1 ]
Empel, Claire [1 ,2 ]
Pei, Chao [1 ]
Vinh Nguyen, Thanh [2 ]
Koenigs, Rene M. [1 ,2 ]
机构
[1] Rhein Westfal TH Aachen, Inst Organ Chem, Landoltweg 1, D-52074 Aachen, Germany
[2] Univ New South Wales, Sch Chem, Sydney, NSW, Australia
基金
澳大利亚研究理事会;
关键词
C-H functionalization; Gold; Phenothiazine; Diazo compounds; Carbenes; SENSITIZED SOLAR-CELLS; BOND FUNCTIONALIZATION; CARBENE; PHENOLS; DERIVATIVES; PERFORMANCE; C(SP(2))-H; AMINATION; INSERTION; LIGAND;
D O I
10.1002/adsc.202000962
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Phenothiazine is an important structural motif in pharmaceuticals and advanced functional organic materials. However, the C-H functionalization reaction of N-protected phenothiazine is rather unexplored and often shadowed by its chemical reactivity on the heteroatomic centers, which limits the diversity of its potential applications. This report demonstrates a straightforward approach towards the site-selective C-H functionalization of phenothiazine at the para-position of N atom via gold-catalyzed carbene transfer reactions (37 examples, up to 83% yield). The mechanism behind the regionselectivity of the C-H functionalization reaction was also elucidated by a combination of computational and experimental studies.
引用
收藏
页码:5721 / 5727
页数:7
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