Rapid and Efficient Microwave-Assisted Amination of Electron-Rich Aryl Halides without a Transition-Metal Catalyst

2003 ◽  
Vol 5 (19) ◽  
pp. 3515-3517 ◽  
Author(s):  
Lei Shi ◽  
Min Wang ◽  
Chun-An Fan ◽  
Fu-Min Zhang ◽  
Yong-Qiang Tu
ChemInform ◽  
2004 ◽  
Vol 35 (4) ◽  
Author(s):  
Lei Shi ◽  
Min Wang ◽  
Chun-An Fan ◽  
Fu-Min Zhang ◽  
Yong-Qiang Tu

2018 ◽  
Vol 42 (13) ◽  
pp. 10989-10992 ◽  
Author(s):  
Arash Ghorbani-Choghamarani ◽  
Zahra Taherinia

A green and efficient methodology for the coupling of aryl halides without the addition of a transition metal catalyst has been presented.


2006 ◽  
Vol 84 (11) ◽  
pp. 1529-1533 ◽  
Author(s):  
Yi-Ju Cao ◽  
Yuan-Yuan Lai ◽  
Hong Cao ◽  
Xiao-Ning Xing ◽  
Xiang Wang ◽  
...  

An efficient carbon–sulfur bond formation reaction has been developed under microwave irradiation. This reaction affords a novel and rapid synthesis of thioacetals and sulfides under mild conditions. This method is particularly noteworthy given its experimental simplicity and high generality, and no transition-metal catalysts were needed under our conditions.Key words: microwave, sulfide, thiol, nucleophilic substitution.


2021 ◽  
Author(s):  
Yingqiu Gu ◽  
Di Xu ◽  
Yun Huang ◽  
Zhouyang Long ◽  
Guojian Chen

Transition metals have been considered as potential catalysts for ammonia decomposition to produce COx-free hydrogen for fuel cells. However, the facile synthesis of transition metal catalyst with small size active...


2021 ◽  
Author(s):  
Zhiqiang Liu ◽  
Goutam Kumar Kole ◽  
Yudha P. Budiman ◽  
Ya-Ming Tian ◽  
Alexandra Friedrich ◽  
...  

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