23866-67-3Relevant articles and documents
Study on Palladium(II)-Catalyzed Mono-1-alkenylation of 9 H -Carbazoles
Guo, Dongdong,Li, Bin,Gao, Wenmei,Zhang, Wuxia,Wang, Yongqiang,Zhao, Jinzhong
, p. 800 - 804 (2021)
A general and efficient method is reported for the direct mono-1-alkenylation of 9 H -carbazole molecules with divalent palladium as a catalyst and an N -(2-pyridyl)sulfanyl directing group. This method also provides an efficient synthetic route for the s
Color tuning based on a six-membered chelated iridium(III) complex with aza-aromatic ligand
Zhu, Rui,Lin, Jian,Wen, Gui-An,Liu, Shu-Juan,Wan, Jun-Hua,Feng, Jia-Chun,Fan, Qu-Li,Zhong, Gao-Yu,Wei, Wei,Huang, Wei
, p. 1668 - 1669 (2005)
A six-membered chelated iridium complex containing aza-aromatic ligand is prepared. Emission color tuning from yellow to deep red is observed for electroluminescent devices with different doping concentrations. Copyright
Palladium-Catalyzed Pyridine-Directed Regioselective Oxidative C–H Acylation of Carbazoles by Using Aldehydes as the Acyl Source
Maiti, Subhadip,Burgula, Laxminarayana,Chakraborti, Gargi,Dash, Jyotirmayee
, p. 332 - 340 (2017)
We herein report a highly regioselective reaction for the palladium-catalyzed oxidative acylation of carbazole derivatives with various aromatic and aliphatic aldehydes as the acyl source. The carbazole derivatives are N-protected with an easily removable pyridine moiety, which directs the Pd-catalyzed ortho acylation to occur at the C-1 and C-8 positions. The reactions of dibromo- and diiodo-substituted N-pyridylcarbazole derivatives, however, provide only the 1-acylated products. This method can be applied to a broad scope of substrates. A reaction mechanism has also been proposed.
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Gilman,Honeycutt
, p. 226 (1957)
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Palladium-catalyzed C-H bond activation for the assembly of: N -aryl carbazoles with aromatic amines as nitrogen sources
Liu, Xiaobing,Sheng, Heyun,Zhou, Yao,Song, Qiuling
supporting information, p. 1665 - 1668 (2020/02/18)
A convenient and efficient palladium-catalyzed C-H bond activation for the assembly of N-aryl carbazole is reported, in which two C-N bonds were formed under one set of conditions. The desired carbazoles were achieved in decent yields with a wide substrate scope by utilizing readily available 2-iodo biphenyls and aromatic amines as starting materials.