scholarly journals Direct synthesis of amides and imines by dehydrogenative homo or cross-coupling of amines and alcohols catalyzed by Cu-MOF

RSC Advances ◽  
2021 ◽  
Vol 11 (34) ◽  
pp. 20788-20793
Author(s):  
Soheil Zamani Anbardan ◽  
Javad Mokhtari ◽  
Ahmad Yari ◽  
Abolfazl Hassani Bozcheloei

Oxidative dehydrogenative homo or cross-coupling of amines with alcohols to imines and amides was achieved with high to moderate yields at room temperature using Cu-MOF as an efficient and recyclable heterogeneous catalyst.

2018 ◽  
Vol 73 (9) ◽  
pp. 641-645 ◽  
Author(s):  
Sepehr Sadegh-Samiei ◽  
Shahrzad Abdolmohammadi

AbstractA novel and efficient synthesis of eight 5-aryl-1,3-dimethyl-2,4-dioxo-1,2,3,4,5,8-hexahydropyrido[2,3-d]pyrimidine-7-carboxylic acids using a TiO2/SiO2 nanocomposite with a molar ratio of 1:1 as a recyclable heterogeneous catalyst is described. The desired products, five of which are new, are formed in short reaction times (2–3 h) with high to excellent yields (94%–98%) under very moderate reaction conditions (room temperature, aqueous media).


Molecules ◽  
2019 ◽  
Vol 24 (15) ◽  
pp. 2714 ◽  
Author(s):  
Matteo Savastano ◽  
Paloma Arranz-Mascarós ◽  
Maria Paz Clares ◽  
Rafael Cuesta ◽  
Maria Luz Godino-Salido ◽  
...  

A new G-(H2L)-Pd heterogeneous catalyst has been prepared via a self-assembly process consisting in the spontaneous adsorption, in water at room temperature, of a macrocyclic H2L ligand on graphene (G) (G + H2L = G-(H2L)), followed by decoration of the macrocycle with Pd2+ ions (G-(H2L) + Pd2+ = G-(H2L)-Pd) under the same mild conditions. This supramolecular approach is a sustainable (green) procedure that preserves the special characteristics of graphene and furnishes an efficient catalyst for the Cu-free Sonogashira cross coupling reaction between iodobenzene and phenylacetylene. Indeed, G-(H2L)-Pd shows an excellent conversion (90%) of reactants into diphenylacetylene under mild conditions (50 °C, water, aerobic atmosphere, 14 h). The catalyst proved to be reusable for at least four cycles, although decreasing yields down to 50% were observed.


2016 ◽  
Vol 40 (6) ◽  
pp. 5053-5060 ◽  
Author(s):  
Shweta Kumari ◽  
Amiya Shekhar ◽  
Devendra D. Pathak

GO–TiO2 has been found to be a highly efficient and recyclable heterogeneous catalyst for the synthesis of pyrazoles and pyridines in aqueous medium at room temperature.


RSC Advances ◽  
2017 ◽  
Vol 7 (88) ◽  
pp. 55756-55766 ◽  
Author(s):  
Chung K. Nguyen ◽  
Hoang H. Vu ◽  
Ha V. Dang ◽  
Ngon N. Nguyen ◽  
Nhan T. H. Le ◽  
...  

CuFe2O4 superparamagnetic nanoparticles were utilized as a recyclable heterogeneous catalyst for the direct synthesis of chemical structures containing both phenol ester and benzothiazole moieties via cross dehydrogenative coupling reactions.


2008 ◽  
Vol 86 (8) ◽  
pp. 841-845 ◽  
Author(s):  
Hamid Reza Shaterian ◽  
Majid Ghashang ◽  
Nassrin Tajbakhsh Riki ◽  
Manijeh Asadi

A highly efficient and mild procedure for the trimethylsilylation of a wide variety of alcohols, including primary, benzylic, secondary, hindered secondary, tertiary, phenols, and oximes with hexamethyldisilazane (HMDS), using Al(H2PO4)3 as a recyclable heterogeneous catalyst at room temperature in a few minutes with excellent yields under solvent-free conditions is described.Key words: trimethylsilylation, hexamethyldisilazane, aluminum tris(dihydrogen phosphate) [Al(H2PO4)3], solvent-free, hydroxyl groups.


RSC Advances ◽  
2018 ◽  
Vol 8 (12) ◽  
pp. 6288-6292 ◽  
Author(s):  
Wei Feng ◽  
Tingting Huang ◽  
Liqian Gao ◽  
Xianfeng Yang ◽  
Wenbin Deng ◽  
...  

A novel textile-supported nanosilver (TsNS) catalyst was prepared and applied in nitroaromatic reduction with excellent activity, stability and recyclability.


RSC Advances ◽  
2014 ◽  
Vol 4 (86) ◽  
pp. 46075-46083 ◽  
Author(s):  
Susmita Roy ◽  
Tanmay Chatterjee ◽  
Biplab Banerjee ◽  
Noor Salam ◽  
Asim Bhaumik ◽  
...  

A Cu(ii)-grafted covalent imine framework material has been designed, which catalyzes the C–Se cross-coupling reactions to obtain a library of organoselenides.


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