56987-44-1Relevant academic research and scientific papers
Terbium–organic framework as heterogeneous Lewis acid catalyst for β-aminoalcohol synthesis: Efficient, reusable and green catalytic method
Karimi, Meghdad,Hajiashrafi, Taraneh,Heydari, Akbar,Azhdari Tehrani, Alireza
, (2017)
A terbium–organic framework (Tb-MOF) was prepared using a previously reported procedure. Tb-MOF was characterized using Fourier transform infrared spectroscopy, scanning electron microscopy, powder X-ray diffraction and surface area analysis. Tb-MOF was e
Tb2(WO4)3@N-GQDs-FA as an efficient nanocatalyst for the efficient synthesis of β-aminoalcohols in aqueous solution
Azizi, Sajjad,Darroudi, Mahdieh,Soleymani, Jafar,Shadjou, Nasrin
, (2021/02/12)
In the current study, Tb2(WO4)3@N-(GQDs) modified with folic acid (FA) was synthesized during the chemical reaction of terbium (III) tungstate nanoparticles with nitrogen doped graphene quantum dots (N-GQDs) and introduced
Heterocyclization Approach for Electrooxidative Coupling of Functional Primary Alkylamines with Aromatics
Morofuji, Tatsuya,Shimizu, Akihiro,Yoshida, Jun-Ichi
, p. 9816 - 9819 (2015/08/24)
A new approach for electrooxidative coupling of aromatic compounds and primary alkylamines bearing a functional group such as a hydroxyl group and an amino group was developed. The key to the success of the transformation is heterocyclization of functional primary alkylamines. Treatment of primary alkylamines bearing a functional group with nitriles or their equivalents gives the corresponding heterocycles. The electrochemical oxidation of aromatic substrates in the presence of the heterocycles followed by chemical reaction under nonoxidative conditions gave the desired coupling products.
Thiourea catalyzed aminolysis of epoxides under solvent free conditions. Electronic control of regioselective ring opening
Chimni, Swapandeep Singh,Bala, Neeraj,Dixit, Vaibhav A.,Bharatam, Prasad V.
experimental part, p. 3042 - 3049 (2010/06/14)
A reactant economizing process for the regioselective aminolysis of epoxides using equimolar quantities of reactants catalyzed by the double hydrogen bond donor N,N′-bis[3,5-bis(trifluoromethyl)phenyl]thiourea is reported. Regioselectivity of the reaction
B2O3/Al2O3 as an efficient and recyclable catalyst for the synthesis of β-amino alcohols under solvent-free conditions
Zhang, Changfu,Chen, Jiuxi,Yu, Xiaochun,Chen, Xian,Wu, Huayue,Yu, Jianping
, p. 1875 - 1887 (2008/09/20)
A convenient and efficient procedure for the solvent-free synthesis of β-amino alcohols has been achieved via B2O3/Al2O3-promoted highly regioselective ring opening of epoxides with aromatic amines in good to excellent yields at room temperature. Addition
