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Nitroalkanes as electrophiles: synthesis of triazole-fused heterocycles with neuroblastoma differentiation activity. Nicolai A. Aksenov, Alexander V. Aksenov, Nikita K. Kirilov, Nikolai A. Arutiunov, Dmitrii A. Aksenov, Vladimir Maslivetc, Zhenze Zhao, Liqin Du, Michael Rubin, Alexander Kornienko , Org. Biomol. Chem. , 2020 , 18 , 6651

Assessment of certain ionic liquids for separation of binary mixtures based on gamma infinity data measurements. M. Karpińska, M. Wlazło, D. Ramjugernath, P. Naidoo, U. Domańska , RSC Adv. , 2017 , 7 , 7092

Complexes of the platinum metals. Part 31. Reactions of binuclear ruthenium(II,III) and rhodium(II) carboxylates with chelating diphosphines;X-ray crystal structure of (acetato-O,O′)bis[bis(diphenylphosphino)methane-P,P′]ruthenium(II) tetraphenylborate. Esther B. Boyar, P. Alexander Harding, Stephen D. Robinson, Carolyn P. Brock , J. Chem. Soc., Dalton Trans. , 1986 , 1771

Electrophilically activated nitroalkanes in reaction with aliphatic diamines en route to imidazolines. Alexander V. Aksenov, Nicolai A. Aksenov, Nikolai A. Arutiunov, Vladimir V. Malyuga, Sergey N. Ovcharov, Michael Rubin , RSC Adv. , 2019 , 9 , 39458

Index of subjects, 1947 , J. Chem. Soc. , 1947 , 1720

Nitro- and fluoro-substituted tetraphenyl–phenyl grafted polysiloxanes as stationary phase for capillary gas chromatography. Jingchen Liu, Li Xu, Jianchun Bai, Aiqin Du, Bo Wu , New J. Chem. , 2019 , 43 , 8290

Aromatic nucleophilic substitution of hydrogen: reactions of 6-nitroquinoline with potassium cyanide and nitroalkanes. Aleš Halama, Vladimír Macháček , J. Chem. Soc., Perkin Trans. 1 , 1999 , 2495

The kinetics and mechanism of the acid-catalysed hydrolysis of nitroalkanes. R. B. Cundall, A. W. Locke , J. Chem. Soc. B , 1968 , 98

Thermal decomposition of the nitroalkanes. Peter Gray, A. D. Yoffe, L. Roselaar , Trans. Faraday Soc. , 1955 , 51 , 1489

Thermodynamics of a food macromolecular assembly: the case of okra mucilage. Maria Dimopoulou, Ioannis Tsivintzelis, Christos Ritzoulis, Costas Panayiotou , RSC Adv. , 2016 , 6 , 20916