scholarly journals Precise through-space control of an abiotic electrophilic aromatic substitution reaction

2017 ◽  
Vol 8 (1) ◽  
Author(s):  
Kyle E. Murphy ◽  
Jessica L. Bocanegra ◽  
Xiaoxi Liu ◽  
H.-Y. Katharine Chau ◽  
Patrick C. Lee ◽  
...  
2009 ◽  
Vol 7 (1) ◽  
pp. 138-142 ◽  
Author(s):  
Ghasem Bardajee ◽  
Farnaz Jafarpour

AbstractIn this report, we described the synthesis and characterization of a variety of diaminotriarylmethane derivatives with dimethylamino functional groups. These compounds were synthesized by the tandem regio-selective electrophilic aromatic substitution reaction of N,N-dimethylaniline with aryl aldehydes to form the corresponding diaminotriarylmethane compounds. In our strategy, Bi(NO3)3 was used as a catalyst under solvent free conditions to afford the desired products in good to excellent yields.


2016 ◽  
Vol 32 (1) ◽  
pp. 253-260 ◽  
Author(s):  
Hasan Obayes ◽  
Khalida Al.Azawi ◽  
Shaymaa Khazaal ◽  
Ghadah Alwan ◽  
Abdulnasser AL-Gebori ◽  
...  

2015 ◽  
Vol 51 (62) ◽  
pp. 12474-12477 ◽  
Author(s):  
Jared B. DeCoste ◽  
Matthew A. Browe ◽  
George W. Wagner ◽  
Joseph A. Rossin ◽  
Gregory W. Peterson

Chlorine gas is removed from airstreams with an amine functionalized metal–organic framework via an electrophilic aromatic substitution reaction producing HCl, which is subsequently neutralized by the substrate.


Synlett ◽  
2017 ◽  
Vol 28 (16) ◽  
pp. 2159-2162 ◽  
Author(s):  
Guangxin Gu ◽  
Hao Guo ◽  
Yang Li ◽  
Yu Wang ◽  
Dawen Xu ◽  
...  

Herein, we wish to report the main-group metal Lewis acid catalyzed intramolecular hydroarylation of arenes with alkynes. This cyclization proceeds efficiently in the presence of a catalytic amount of AlCl3, affording phenanthrenes in moderate to excellent yields. The catalyst is cheap and nontoxic. The functional-group tolerance is high. A plausible electrophilic aromatic substitution reaction mechanism is proposed for this transformation.


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