Copper-Catalyzed One-Pot Synthesis of Functionalized Pyrroles from Sulfonyl Azides, Alkynes, and (p-Toluenesulfonyl)methyl Isocyanide

2013 ◽  
Vol 96 (11) ◽  
pp. 2098-2102 ◽  
Author(s):  
Issa Yavari ◽  
Manijeh Nematpour



2012 ◽  
Vol 53 (8) ◽  
pp. 942-943 ◽  
Author(s):  
Issa Yavari ◽  
Manijeh Nematpour ◽  
Majid Ghazanfarpour-Darjani


ChemInform ◽  
2012 ◽  
Vol 43 (6) ◽  
pp. no-no
Author(s):  
Hojat Veisi ◽  
Ramin Ghorbani-Vaghei ◽  
Saba Hemmati ◽  
Jafar Mahmoodi


2013 ◽  
Vol 96 (12) ◽  
pp. 2214-2217 ◽  
Author(s):  
Issa Yavari ◽  
Tahereh Damghani ◽  
Manijeh Nematpour


ChemInform ◽  
2012 ◽  
Vol 43 (24) ◽  
pp. no-no
Author(s):  
Issa Yavari ◽  
Manijeh Nematpour ◽  
Majid Ghazanfarpour-Darjani


ChemInform ◽  
2012 ◽  
Vol 43 (9) ◽  
pp. no-no
Author(s):  
Yao Li ◽  
Deng Hong ◽  
Yuanxun Zhu ◽  
Ping Lu ◽  
Yanguang Wang


Molecules ◽  
2021 ◽  
Vol 26 (12) ◽  
pp. 3700
Author(s):  
Yu Zhao ◽  
Zitong Zhou ◽  
Man Chen ◽  
Weiguang Yang

N-Sulfonyl amidines are developed from a Cu-catalyzed three-component reaction from sulfonyl hydrazines, terminal alkynes and sulfonyl azides in toluene at room temperature. Particularly, the intermediate N-sulfonylketenimines was generated via a CuAAC/ring-opening procedure and took a nucleophilic addition with the weak nucleophile sulfonyl hydrazines. In addition, the stability of the product was tested by a HNMR spectrometer.



ChemInform ◽  
2014 ◽  
Vol 45 (13) ◽  
pp. no-no
Author(s):  
Behrooz Maleki ◽  
et al. et al.


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