Ionic Liquids as (Co-)Solvents and Co-Catalysts for Organocatalytic Reactions

Author(s):  
Štefan Toma ◽  
Radovan Šebesta
2015 ◽  
Vol 69 (5) ◽  
Author(s):  
Melinda Mojzesová ◽  
Mária Mečiarová ◽  
Ambroz Almássy ◽  
Roger Marti ◽  
Radovan Šebesta

AbstractNon-standard experimental conditions can often enhance organocatalytic reactions considerably. The current study explores the effectiveness of a range of non-standard reaction conditions for the asymmetric organocatalytic 1,3-dipolar cycloaddition of a nitrone with α,β-unsaturated aldehydes. The influence of ionic liquids, high-pressure conditions, ultrasound, microwave irradiation and ballmilling was tested as well as the flow process. Because of the low reactivity of the nitrone and unsaturated aldehydes in the 1,3-dipolar cycloaddition, cycloadducts were isolated in only moderate yields from the majority of experiments. However, high diastereo- and enantioselectivities were observed in ionic liquids under solvent-free conditions and in the flow reactor.


2018 ◽  
Vol 42 (1) ◽  
pp. 228-236 ◽  
Author(s):  
Komal Kumar ◽  
Firdaus Parveen ◽  
Tanmoy Patra ◽  
Sreedevi Upadhyayula

An efficient catalytic system comprising Bronsted acidic ionic liquids and Lewis acidic metal salts for hydrothermal glucose conversion to platform chemicals.


ChemInform ◽  
2009 ◽  
Vol 40 (13) ◽  
Author(s):  
Stefan Toma ◽  
Maria Meciarova ◽  
Radovan Sebesta

2009 ◽  
Vol 2009 (3) ◽  
pp. 321-327 ◽  
Author(s):  
Štefan Toma ◽  
Mária Mečiarová ◽  
Radovan Šebesta

Catalysts ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 262
Author(s):  
Francesca Valentini ◽  
Giacomo Ferracci ◽  
Pierluca Galloni ◽  
Giuseppe Pomarico ◽  
Valeria Conte ◽  
...  

Thanks to the well-recognized role of benzaldehyde in industry, nowadays the research of new and sustainable approaches to selectively synthesize such an interesting product is receiving great attention from the chemists’ community. In this paper, a V-based catalytic biphasic system is adopted to perform toluene oxidation to benzaldehyde. Importantly, to pursue sustainability, organic solvents have been avoided, so toluene is used as substrate and co-solvent, together with water. Also, the use of hydrophobic ionic liquids has been explored. To perform oxidation, NH4VO3 catalyst, H2O2, and a safe and inexpensive co-catalyst are used. Among the tested co-catalysts, KF and O2 were found to be the best choice, to guarantee good yields, in mild reaction conditions. In fact, with such a sustainable method, up to 30% of benzaldehyde can be obtained at 60 °C and, more interestingly, the oxidative system can be recharged, raising-up the yield. The entire process results highly selective, since no traces of benzyl alcohol or benzoic acid are detected. Hence, it constitutes a very appealing synthetic route, even suitable to be easily scaled-up at an industrial level.


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