Issues concerning the use of renewable Ca-based solids as transesterification catalysts

Fuel ◽  
2015 ◽  
Vol 158 ◽  
pp. 558-564 ◽  
Author(s):  
Inés Reyero ◽  
Fernando Bimbela ◽  
Alberto Navajas ◽  
Gurutze Arzamendi ◽  
Luis M. Gandía
2011 ◽  
Vol 49 (24) ◽  
pp. 5301-5312 ◽  
Author(s):  
Nicolas Jacquel ◽  
Floriane Freyermouth ◽  
Françoise Fenouillot ◽  
Alain Rousseau ◽  
Jean Pierre Pascault ◽  
...  

Synlett ◽  
1999 ◽  
Vol 1999 (Sup. 1) ◽  
pp. 957-959 ◽  
Author(s):  
Norman Lewis ◽  
Christina Ribas ◽  
Andrew Wells

2013 ◽  
Vol 49 (73) ◽  
pp. 8006 ◽  
Author(s):  
Guiju Tao ◽  
Zile Hua ◽  
Zhe Gao ◽  
Yan Zhu ◽  
Yan Zhu ◽  
...  

2016 ◽  
Vol 12 ◽  
pp. 1911-1924 ◽  
Author(s):  
Maurizio Selva ◽  
Alvise Perosa ◽  
Sandro Guidi ◽  
Lisa Cattelan

The use of ionic liquids (ILs) as organocatalysts is reviewed for transesterification reactions, specifically for the conversion of nontoxic compounds such as dialkyl carbonates to both linear mono-transesterification products or alkylene carbonates. An introductory survey compares pros and cons of classic catalysts based on both acidic and basic systems, to ionic liquids. Then, innovative green syntheses of task-specific ILs and their representative applications are introduced to detail the efficiency and highly selective outcome of ILs-catalyzed transesterification reactions. A mechanistic hypothesis is discussed by the concept of cooperative catalysis based on the dual (electrophilic/nucleophilic) activation of reactants.


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