Theoretical Study of Plasmon-Enhanced Surface Catalytic Coupling Reactions of Aromatic Amines and Nitro Compounds

2014 ◽  
Vol 5 (7) ◽  
pp. 1259-1266 ◽  
Author(s):  
Liu-Bin Zhao ◽  
Meng Zhang ◽  
Yi-Fan Huang ◽  
Christopher T. Williams ◽  
De-Yin Wu ◽  
...  
Synlett ◽  
2021 ◽  
Author(s):  
Tran Quang Hung ◽  
Tuan Thanh Dang ◽  
Peter Langer ◽  
Ha Nam Do ◽  
Nguyen Minh Quan ◽  
...  

AbstractAn efficient Cu-catalyzed synthesis of carbazole derivatives is reported, which proceeds by double C–N coupling reactions of 2,2′-dibromobiphenyl and amines in the presence of air. The reaction is robust, proceeds in high yields, and tolerates a series of amines including neutral, electron-rich, electron-deficient aromatic amines and aliphatic amines.


1973 ◽  
Vol 50 (4) ◽  
pp. 989-995 ◽  
Author(s):  
Jack L. Radomski ◽  
Gaylord M. Conzelman ◽  
Alberto A. Rey ◽  
Earl Brill

ChemInform ◽  
2016 ◽  
Vol 47 (42) ◽  
Author(s):  
Hongtao Lu ◽  
Zhiyue Geng ◽  
Jingya Li ◽  
Dapeng Zou ◽  
Yusheng Wu ◽  
...  

2011 ◽  
Vol 2011 ◽  
pp. 1-7 ◽  
Author(s):  
Mantu Rajbangshi ◽  
Md. Rumum Rohman ◽  
Icydora Kharkongor ◽  
Hormi Mecadon ◽  
Bekington Myrboh

Iodine-alumina was employed as a catalyst in the coupling reactions of aldehydes, enolizable ketones, or 1,3-dicarbonyls with methyl carbamate or aromatic amines under microwave irradiation to afford β-amino carbonyl compounds in good-to-excellent yields. The key features of this environmentally friendly methodology are its operational simplicity, mild reaction conditions, and less reaction time.


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