Transition-metal-free synthesis of vinyl sulfones via tandem cross-decarboxylative/coupling reactions of sodium sulfinates and cinnamic acids

2014 ◽  
Vol 16 (8) ◽  
pp. 3720-3723 ◽  
Author(s):  
Yanli Xu ◽  
Xiaodong Tang ◽  
Weigao Hu ◽  
Wanqing Wu ◽  
Huanfeng Jiang

A transition-metal-free synthesis of vinyl sulfones, utilizing sodium sulfinates and cinnamic acids through tandem cross-decarboxylative/coupling reactions, has been developed.

2016 ◽  
Vol 5 (9) ◽  
pp. 1148-1154 ◽  
Author(s):  
Francis Mariaraj Irudayanathan ◽  
Jimin Kim ◽  
Kwang Ho Song ◽  
Sunwoo Lee

Synlett ◽  
2021 ◽  
Author(s):  
Yadong Sun ◽  
Ablimit Abdukader ◽  
Yuhan Lu ◽  
Chenjiang Liu

AbstractA highly efficient method for the synthesis of 1,2,3-thiadiazoles has been developed by utilizing readily available tosylhydrazones and ammonium thiocyanate with ecofriendly EtOH as the solvent at room temperature. The reaction shows a wide scope of substrates and good functional-group tolerance. This protocol can be scaled up to a gram level and can be applied to coupling reactions with 4-(4-bromophenyl)-1,2,3-thiadiazole as the substrate.


2018 ◽  
Vol 7 (6) ◽  
pp. 1118-1123 ◽  
Author(s):  
Miao Lai ◽  
Yuan Li ◽  
Zhiyong Wu ◽  
Mingqin Zhao ◽  
Xiaoming Ji ◽  
...  

2003 ◽  
Vol 42 (12) ◽  
pp. 1407-1409 ◽  
Author(s):  
Nicholas E. Leadbeater ◽  
Maria Marco

2014 ◽  
Vol 114 (18) ◽  
pp. 9219-9280 ◽  
Author(s):  
Chang-Liang Sun ◽  
Zhang-Jie Shi

ChemInform ◽  
2016 ◽  
Vol 47 (45) ◽  
Author(s):  
Shunyou Cai ◽  
Yaohui Xu ◽  
Danling Chen ◽  
Lihuang Li ◽  
Qifa Chen ◽  
...  

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