Synthesis of Fluorescent Indazoles by Palladium-Catalyzed Benzannulation of Pyrazoles with Alkynes

被引:45
|
作者
Kim, Og Soon [1 ]
Jang, Jin Hyeok [1 ]
Kim, Hyun Tae [1 ]
Han, Su Jin [1 ]
Tsui, Gavin Chit [2 ]
Joo, Jung Min [1 ]
机构
[1] Pusan Natl Univ, Inst Funct Mat, Dept Chem & Chem, Busan 46241, South Korea
[2] Chinese Univ Hong Kong, Dept Chem, Shatin, Hong Kong, Peoples R China
基金
新加坡国家研究基金会;
关键词
C-H ACTIVATION; UNSYMMETRICAL DIARYLALKYNES; UBIQUITOUS FUNCTIONALITY; COUPLING REACTIONS; DIRECT ARYLATIONS; INTERNAL ALKYNES; GENERAL-APPROACH; DIRECTING GROUP; PROPIOLIC ACID; BOND FORMATION;
D O I
10.1021/acs.orglett.7b00410
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The synthesis of indazoles from pyrazoles and internal alkynes is described. Instead of complex benzenoid compounds, readily available pyrazoles were used for the preparation of indazoles by reaction of the C-H bonds of the heterocyclic ring. Oxidative benzannulation was also applied to imidazoles, providing benzimidazoles. This convergent strategy enabled alteration of the photochemical properties of benzo-fused diazoles by varying the substituents at the benzene ring, thus leading to the development of tetraarylindazoles as new fluorophores.
引用
收藏
页码:1450 / 1453
页数:4
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