A Mild, One-Pot Synthesis of ArylaminesviaPalladium- Catalyzed Addition of Aryl Aldehydes with Amines and Arylboronic Acids in Water

2009 ◽  
Vol 351 (5) ◽  
pp. 767-771 ◽  
Author(s):  
Ajuan Yu ◽  
Yangjie Wu ◽  
Baoli Cheng ◽  
Kun Wei ◽  
Jingya Li
2011 ◽  
Vol 76 (11) ◽  
pp. 1307-1315 ◽  
Author(s):  
Behrooz Maleki ◽  
Hafezeh Salehabadi ◽  
Zeinalabedin Sepehr ◽  
Mina Kermanian

A simple and benign protocol has been explored for the preparation of 2,4,6-triarylpyridines by a one-pot reaction between aryl aldehydes, enolizable ketones and ammonium acetate in the presence of N-bromosuccinimide or trichloroisocyanuric acid as green and neutral catalysts. The reactions proceed smoothly at 130 °C under solvent-free conditions to provide 2,4,6-triarylpyridines in good yields.


ChemInform ◽  
2016 ◽  
Vol 47 (12) ◽  
pp. no-no
Author(s):  
Changbo Hao ◽  
Changjian Zhou ◽  
Jianwei Xie ◽  
Jie Zhang ◽  
Ping Liu ◽  
...  

Author(s):  
Abhilash Sharma ◽  
Dhiraj Dutta ◽  
Pranjal Gogoi

A palladium-catalyzed synthetic strategy has been developed for one-pot synthesis of functionalized spiro(indoline-3,2′-quinazolin)-2-one derivatives from 2-aminobenzonitriles, arylboronic acids and isatins. This cascade strategy proceeds via successive C–C and two C–N bond formations in a single reaction vessel.


2019 ◽  
Vol 77 (12) ◽  
pp. 1263
Author(s):  
Xiaochun Zhao ◽  
Tianqi Ding ◽  
Lüqi Jiang ◽  
Wenbin Yi

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