LaCl3⋅7H2O as an Effective Catalyst for the Synthesis of α-Aminophosphonates under Solvent-Free Conditions and Docking Simulation of Ligand Bond Complexes of Cyclin-Dependent Kinase 2

Author(s):  
Mahdi Mirzaei ◽  
Hossein Eshghi ◽  
Reihaneh Sabbaghzadeh
RSC Advances ◽  
2016 ◽  
Vol 6 (25) ◽  
pp. 20687-20694 ◽  
Author(s):  
R. Tayebee ◽  
B. Maleki ◽  
F. M. Zonoz ◽  
R. M. Kakhki ◽  
T. Kunani

H7[(P2W17O61)FeIII(H2O)] is introduced as an effective catalyst for the one-pot synthesis ofN,N′-alkylidenebisamides. The catalyst could be easily separated without noticeable reduction in activity.


Author(s):  
Ruiyang Qu ◽  
Margherita Macino ◽  
Sarwat Iqbal ◽  
Xiang Gao ◽  
Qian He ◽  
...  

Selective hydrogenation of nitrobenzene was carried out under solvent-free conditions using supported AuPd nanoparticles catalyst, prepared by modified impregnation method (MIm), as efficient catalyst. >99% yield of aniline (AN) was obtained after 15 hours at 90 °C, 3 bar H2 that can be used without any further purification or separation, therefore reducing cost and energy input. Supported AuPd nanoparticles catalyst, prepared by MIm, was found to be active and stable even after 4 recycle experiments whereas the same catalyst prepared by SIm deactivated during the recycle experiments. The most effective catalyst was tested for the chemoselective hydrogenation of 4-chloronitrobenzene (CNB) to 4-chloroaniline (CAN). The activation energy of CNB to CAN was found to be 25 kJ mol-1, while that of CNB to AN was found to be 31 kJ mol-1. Based on this, the yield of CAN was maximized (92%) by lowering the reaction temperature to 25 °C.


ChemInform ◽  
2008 ◽  
Vol 39 (51) ◽  
Author(s):  
Minoo Dabiri ◽  
Mostafa Baghbanzadeh ◽  
Seyedeh C. Azimi ◽  
Shaghayegh Ahmadzadeh-Asl ◽  
Reza R. Ardestani

RSC Advances ◽  
2019 ◽  
Vol 9 (9) ◽  
pp. 5158-5163 ◽  
Author(s):  
Hongshe Wang ◽  
Weixing Zhao ◽  
Juan Du ◽  
Fenyan Wei ◽  
Qi Chen ◽  
...  

A simple and efficient protocol developed for one pot three-component synthesis of 2,4,6-triarylpyridines from aromatic aldehydes, substituted acetophenones and ammonium acetate using triflimide (HNTf2) as an effective catalyst is described.


2016 ◽  
Vol 2016 ◽  
pp. 1-9 ◽  
Author(s):  
Emel Pelit ◽  
Zuhal Turgut

New 1-[(1,3-thiazol-2-ylamino)methyl]-2-naphthols were obtained by condensation of 2-aminothiazole, aromatic aldehydes, and 2-naphthol in the presence of (+)-camphor-10-sulfonic acid ((+)-CSA) as an effective catalyst under ultrasound-promoted solvent-free conditions. The 1-[(1,3-thiazol-2-ylamino)methyl]-2-naphthol derivatives were converted in ring-closure reaction with formaldehyde to the corresponding naphthoxazine derivatives.


2007 ◽  
Vol 85 (5) ◽  
pp. 336-340 ◽  
Author(s):  
Ardeshir Khazaei ◽  
Amin Rostami ◽  
Ayeh Raiatzadeh ◽  
Marjan Mahboubifar

Structurally diverse alcohols and phenols were trimethylsilylated in a clean and efficient reaction with hexamethyldisilazane (HMDS) based on the use of a catalytic amount of N-bromosuccinimide under both dichloromethane and solvent-free conditions at room temperature. Deprotection of trimethylsilyl ethers was also be achieved efficiently in the presence of a catalytic amount of NBS in methanol at ambient temperature.Key words: N-bromosuccinimide, solvent-free, alcohols, phenols, hexamethyldisilazane, trimethylsilyl ether, catalyst, detrimethylsilylation.


2008 ◽  
Vol 5 (6) ◽  
pp. 490-494 ◽  
Author(s):  
Minoo Dabiri ◽  
Mostafa Baghbanzadeh ◽  
Seyedeh Azimi ◽  
Shaghayegh Ahmadzadeh-Asl ◽  
Reza Ardestani

2018 ◽  
Vol 24 (6) ◽  
pp. 293-296 ◽  
Author(s):  
Huaiyuan Kang ◽  
Weili Wang ◽  
Qinqiang Sun ◽  
Shuya Yang ◽  
Juan Jin ◽  
...  

Abstract Antimony(III) trichloride (SbCl3) is an effective catalyst (1 mol%) for the condensation of anthranilic amide with various aldehydes or ketones to quinazolin-4(3H)-one derivatives in good to excellent yields under microwave irradiation. The process is carried out within several minutes under solvent-free conditions. This general methodology has the advantages of simplicity, mild reaction conditions and high yields of products.


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