New thiosemicarbazide and dithiocarbazate based oxidovanadium(iv) and dioxidovanadium(v) complexes. Reactivity and catalytic potential

2019 ◽  
Vol 43 (45) ◽  
pp. 17620-17635 ◽  
Author(s):  
Mannar R. Maurya ◽  
Bithika Sarkar ◽  
Amit Kumar ◽  
Nádia Ribeiro ◽  
Aistè Miliute ◽  
...  

The new thiosemicarbazide and dithiocarbazate based vanadium complexes show remarkable catalytic potential for oxidation of alcohols and simple arenes.

Nanomaterials ◽  
2019 ◽  
Vol 9 (3) ◽  
pp. 442
Author(s):  
Maciej Kapkowski ◽  
Anna Niemczyk-Wojdyla ◽  
Piotr Bartczak ◽  
Monika Pyrkosz Bulska ◽  
Kamila Gajcy ◽  
...  

The classical stoichiometric oxidation of alcohols is an important tool in contemporary organic chemistry. However, it still requires huge modifications in order to comply with the principles of green chemistry. The use of toxic chemicals, hazardous organic solvents, and the large amounts of toxic wastes that result from the reactions are a few examples of the problems that must be solved. Nanogold alone or conjugated with palladium were supported on different carriers (SiO2, C) and investigated in order to evaluate their catalytic potential for environmentally friendly alcohol oxidation under solvent-free and base-free conditions in the presence H2O2 as a clean oxidant. We tested different levels of Au loading (0.1–1.2% wt.) and different active catalytic site forms (monometallic Au or bimetallic Au–Pd sites). This provided new insights on how the structure of the Au-dispersions affected their catalytic performance. Importantly, the examination of the catalytic performance of the resulting catalysts was oriented toward a broad scope of alcohols, including those that are the most resistant to oxidation—the primary aliphatic alcohols. Surprisingly, the studies proved that Au/SiO2 at a level of Au loading as low as 0.1% wt. appeared to be efficient and prospective catalytic system for the green oxidation of alcohol. Most importantly, the results revealed that 0.1% Au/SiO2 might be the catalyst of choice with a wide scope of utility in the green oxidation of various structurally different alcohols as well as the non-activated aliphatic ones.


2004 ◽  
Vol 357 (2) ◽  
pp. 475-484 ◽  
Author(s):  
Georg Süss-Fink ◽  
Laura Gonzalez Cuervo ◽  
Bruno Therrien ◽  
Helen Stoeckli-Evans ◽  
Georgiy B Shul’pin

2013 ◽  
Vol 42 (33) ◽  
pp. 11941 ◽  
Author(s):  
Mannar R. Maurya ◽  
Chanchal Haldar ◽  
Amit Kumar ◽  
Maxim L. Kuznetsov ◽  
Fernando Avecilla ◽  
...  

2011 ◽  
Vol 32 (1) ◽  
pp. 118-122 ◽  
Author(s):  
Lipeng ZHOU ◽  
Chaofeng ZHANG ◽  
Tao FANG ◽  
Bingbing ZHANG ◽  
Ying WANG ◽  
...  

2019 ◽  
Vol 23 (11) ◽  
pp. 1168-1213 ◽  
Author(s):  
Samar Noreen ◽  
Ameer Fawad Zahoor ◽  
Sajjad Ahmad ◽  
Irum Shahzadi ◽  
Ali Irfan ◽  
...  

Background: Asymmetric catalysis holds a prestigious role in organic syntheses since a long time and chiral inductors such as ligands have been used to achieve the utmost desired results at this pitch. The asymmetric version of Tsuji-Trost allylation has played a crucial role in enantioselective synthesis. Various chiral ligands have been known for Pdcatalyzed Asymmetric Allylic Alkylation (AAA) reactions and exhibited excellent catalytic potential. The use of chiral ligands as asymmetric inductors has widened the scope of Tsuji-Trost allylic alkylation reactions. Conclusion: Therefore, in this review article, a variety of chiral inductors or ligands have been focused for palladium catalyzed asymmetric allylic alkylation (Tsuji-Trost allylation) and in this regard, recently reported literature (2013-2017) has been described. The use of ligands causes the induction of enantiodiscrimination to the allylated products, therefore, the syntheses of various kinds of ligands have been targeted by many research groups to employ in Pd-catalyzed AAA reactions.


2013 ◽  
Vol 2 (2) ◽  
pp. 151-158 ◽  
Author(s):  
Mohammad Ali Zolfigol ◽  
Ali Reza Pourali ◽  
Sami Sajjadifar ◽  
Shohreh Farahmand

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