One-pot synthesis of 2,4,6-triarylpyridines from β-nitrostyrenes, substituted salicylic aldehydes and ammonium acetate

RSC Advances ◽  
2016 ◽  
Vol 6 (98) ◽  
pp. 95957-95964 ◽  
Author(s):  
Xushun Qing ◽  
Ting Wang ◽  
Feixiang Zhang ◽  
Cunde Wang

The diversity-oriented synthesis of 2,4,6-trisubstituted pyridines via K2CO3-promoted multicomponent reactions of the β-nitrostyrenes, available substituted salicylic aldehydes and ammonium acetate have been developed.

2010 ◽  
Vol 185 (7) ◽  
pp. 1395-1403 ◽  
Author(s):  
Ghasem Marandi ◽  
Malek Taher Maghsoodlou ◽  
Reza Heydari ◽  
Sayyed Mostafa Habibi-Khorassani ◽  
Roya Kabiri ◽  
...  

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.


2011 ◽  
Vol 15 (4) ◽  
pp. 911-916 ◽  
Author(s):  
Zinatossadat Hossaini ◽  
Faramarz Rostami-Charati ◽  
Samira Soltani ◽  
Anwar Mirzaei ◽  
Kayhaneh Berijani

Tetrahedron ◽  
2013 ◽  
Vol 69 (32) ◽  
pp. 6541-6544 ◽  
Author(s):  
Arash Ghorbani-Choghamarani ◽  
Maryam Hajjami ◽  
Masoomeh Norouzi ◽  
Yunes Abbasityula ◽  
Václav Eigner ◽  
...  

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