A convenient and eco-friendly synthesis of various fused N-heterocyclic compounds through catalyst and additive-free 1,3 dipolar cycloadditions of quinolinium imides with olefins, maleimides, and benzynes in excellent yields and diastereoselectivities is reported. The thermally controlled diastereoselective [3 + 2] cycloaddition reaction between quinolinium imides and olefins provided cis-isomers at low temperature and trans-isomers at high temperature. A reaction between quinolinium imides with substituted maleimides gave four-ring-fused N-heterocyclic compounds in high yields as a single diastereomer. The aryne precursors also provided four-ring-fused N,N'-heterocyclic compounds in high yields. The in vitro antiplasmodial activity of selected molecules revealed that this class of molecules possesses potential for ongoing studies against malaria.
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http://dx.doi.org/10.1021/acs.joc.8b01520 | DOI Listing |
J Chromatogr A
September 2023
Boreskov Institute of Catalysis, pr. Lavrentieva 5, Novosibirsk 630090, Russia.
The study demonstrates the possibility of using ionic liquids (IL) as a stationary liquid phase (SLP) for gas chromatographic (GC) multicapillary columns (MCC). Three types of IL of three classes were employed as SLP: Imidazolium, Pyridinium and Quinolinium. Dependences of the MCCs efficiency on the carrier gas flow rate were obtained.
View Article and Find Full Text PDFAngew Chem Weinheim Bergstr Ger
July 2022
Herein we disclose a mild protocol for the reductive functionalisation of quinolinium and isoquinolinium salts. The reaction proceeds under transition-metal-free conditions as well as under rhodium catalysis with very low catalyst loadings (0.01 mol %) and uses inexpensive formic acid as the terminal reductant.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
July 2022
Department of Chemistry, University of Oxford, Chemistry Research Laboratory, Mansfield Road, Oxford, OX1 3TA, UK.
Herein we disclose a mild protocol for the reductive functionalisation of quinolinium and isoquinolinium salts. The reaction proceeds under transition-metal-free conditions as well as under rhodium catalysis with very low catalyst loadings (0.01 mol %) and uses inexpensive formic acid as the terminal reductant.
View Article and Find Full Text PDFMolecules
December 2020
Thermodynamics Research Unit, School of Chemical Engineering, University of KwaZulu-Natal, Howard College Campus, King George V Avenue, Durban 4041, South Africa.
Experimental and theoretical studies on thermodynamic properties of quinolinium-based ionic liquids (ILs) based on bis(trifluoromethylsulfonyl)imide anion (namely -butyl-quinoloinium bis(trifluoromethylsulfonyl)imide, [BQuin][NTf], -hexylquinoloinium bis(trifluoromethyl-sulfonyl)imide, [HQuin][NTf], and -octylquinoloinium bis(trifluoromethyl-sulfonyl)imide, [OQuin][NTf]) with aromatic sulfur compounds and heptane, as a model compound of fuel were examined in order to assess the applicability of the studied ionic liquids for desulfurization of fuels. With this aim, the temperature-composition phase diagrams of 13 binary mixtures composed of organic sulfur compounds (thiophene, benzothiophene, or 2-methylthiophene) or heptane and ionic liquid (IL) were investigated at ambient pressure. A dynamic method was used to determine the (solid-liquid) equilibrium phase diagrams in binary systems over a wide composition range and temperature range from = 255.
View Article and Find Full Text PDFJ Mol Model
January 2020
Theoretical and Computational Chemistry Laboratory, Department of Chemistry, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.
This work investigated computationally the regio-, stereo-, and enantio-selectivity of the reactions of azomethine imines with olefins, maleimides, and benzynes, important reactions towards the synthesis of heteropolycyclic, N,N'-fused, spirocyclic systems, which serve as building blocks for the synthesis of many pharmaceuticals, agrochemicals, and biologically active compounds. The results show that the thermally controlled diastereoselective [3 + 2] cycloaddition reaction between quinolinium imide and methyl acrylate provides two regio-isomers: 1,4-regioisomer (N-C1, C-C2) and 1,3-regioisomer (N-C2, C-C1). The 1,4-regioisomer has cis and trans-stereoisomers while the 1,3-regioisomer has R-enantiomer and S-enantiomer, and the barriers for the formation of these isomers are 5.
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