Reactions catalyzed within inorganic and organic materials and at electrochemical interfaces commonly occur at high coverage and in condensed media, causing turnover rates to depend strongly on interfacial structure and composition, 124172-53-8, Name is N,N’-(Hexane-1,6-diyl)bis(N-(2,2,6,6-tetramethylpiperidin-4-yl)formamide), SMILES is O=CN(CCCCCCN(C1CC(C)(C)NC(C)(C)C1)C=O)C2CC(C)(C)NC(C)(C)C2, in an article , author is Fatahpour, Maryam, once mentioned of 124172-53-8, Recommanded Product: 124172-53-8.
One-pot multicomponent synthesis of piperidinium 3,3 ‘-(arylmethylene) bis (2-hydroxynaphthalene-1,4-diones): NMR spectroscopic and X-ray structure characterization
A facile synthesis of piperidinium 3,3’-(arylmethylene) bis (2-hydroxynaphthalene-1,4-dione) analogs as organic salts is described by the one-pot pseudo-four-component reaction between 2-hydroxy-1,4-naphthoquinone, aromatic aldehydes, and piperidine. The single-crystal X-ray diffraction analysis of these systems confirms that the stabilized predominant interactions are N-H center dot center dot center dot O and O-H center dot center dot center dot O hydrogen bonds. Mild and clean reaction conditions, high atom economy, and operational simplicity of this one-pot multicomponent reaction coupled with excellent yields and no need for column chromatography have transformed this procedure to be a superior synthetic route for the efficient formation of families of naphthoquinone-derived compounds.
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Reference:
Piperidine – Wikipedia,
,Piperidine | C5H11N – PubChem