42419-56-7Relevant academic research and scientific papers
Gallic acid-functionalized magnetic nanoparticles: a convenient and green approach for synthesis of α-aminonitriles under solvent-free conditions
Eidi, Esmaiel,Kassaee, Mohamad Z.,Nasresfahani, Zahra,Cummings, Peter T.
, p. 303 - 314 (2018/10/15)
Abstract: Gallic acid-coated magnetic nanoparticles were efficiently prepared, characterized by Fourier transform infrared spectroscopy, X-ray diffraction, vibrating sample magnetometry, scanning electron microscopy, and transmission electron microscopy, and employed as an environmentally friendly and recyclable catalyst for one-pot synthesis of three-component reaction via Strecker reaction, incorporating aldehydes/ketones, amines, and trimethylsilyl cyanides under solvent-free conditions. Operational simplicity, product purity, natural resources and reusability of the catalyst are considered as evident features of this protocol which will hopefully develop into an inexpensive, efficient, and clean strategy for the synthesis of α-aminonitriles. Graphical abstract: [Figure not available: see fulltext.].
Nanostructured oxytyramine catalyst for the facile one-pot synthesis of cyclohexanecarbonitrile derivatives
Arora, Priya,Rajput, Jaspreet Kaur,Singh, Harminder
, p. 97212 - 97223 (2015/11/28)
The magnetic, recyclable heterogeneous organocatalyst OT@Si@SPIONs has been developed in this report, with the aim of synthesizing cyclohexanecarbonitriles. The prepared nanocatalyst was fully characterized by various techniques and its catalytic activity
Magnetic solid sulfonic acid decorated with hydrophobic regulators: A combinatorial and magnetically separable catalyst for the synthesis of α-aminonitriles
Mobaraki, Akbar,Movassagh, Barahman,Karimi, Babak
supporting information, p. 352 - 358 (2014/08/05)
A three-component, Strecker reaction of a series of aldehydes or ketones, amines, and trimethylsilyl cyanide for the synthesis of α-aminonitriles in the presence of a catalytic amount of a magnetic solid sulfonic acid catalyst, Fe3O4@SiO2@Me&Et-PhSO3H under solvent-free conditions have been investigated. This catalyst, with a combination of hydrophobicity and acidity on the Fe3O 4@SiO2 core-shell of the magnetic nanobeads, as well as its water-resistant property, enabled easy mass transfer and catalytic activity in the Strecker reaction. The catalyst was easily separated by an external magnet and the recovered catalyst was reused in 6 successive reaction cycles without any significant loss of activity.
Search for Newer Analgesic Agents: Part I - Synthesis of 1-Arylaminocyclohexane-1-carboxamide Derivatives
Singh, G. B.,Jetley, Aruna,Rathore, H. G. S.
, p. 76 - 77 (2007/10/02)
N-(Substituted aminomethyl)-1-arylaminocyclohexane-1-carboxamides have been synthesized in which nitrogen of the amide group is linked through a methylene side chain with basic fragments like pyrrolidino, piperidino, morpholino, etc.These compounds contai
