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- Theoretical studies on the initial reaction kinetics and mechanisms of p-, m- and o-nitrotoluene. Meng Yang, Caiyue Liao, Chenglong Tang, Peng Zhang, Zuohua Huang, Jianling Li
, Phys. Chem. Chem. Phys.
, 2021
, 23
, 4658
- Competition between electron-donor and electron-acceptor substituents in nitrotoluene isomers: a photoelectron spectroscopy and ab initio investigation. Flaminia Rondino, Daniele Catone, Giuseppe Mattioli, Aldo Amore Bonapasta, Paola Bolognesi, Anna Rita Casavola, Marcello Coreno, Patrick O'Keeffe, Lorenzo Avaldi
, RSC Adv.
, 2014
, 4
, 5272
- Highly selective detection of nitrotoluene based on novel lanthanide-containing ionic liquids. Ling Zheng, Li-Li Yang, Nan-Nan Xing, Yi Pan, Hong-Xiang Ji, Jie Wei, Wei Guan
, RSC Adv.
, 2017
, 7
, 35814
- CCCCXXXIV.—The mercuration of aromatic substances. Part III. p- and m-Nitrotoluenes. Samuel Coffey
, J. Chem. Soc.
, 1926
, 129
, 3215
- High-efficiency cucurbit[7]uril capillary column for gas chromatographic separations of structural and positional isomers. Yan Zhang, Meiling Qi, Ruonong Fu
, RSC Adv.
, 2016
, 6
, 36163
- Negative ion mass spectrometry. Part 2.1—Ionization processes in 2- and 3-nitrotoluene. Roger G. Alexander, David B. Bigley, Robert B. Turner, John F. J. Todd
, J. Chem. Soc., Faraday Trans. 1
, 1974
, 70
, 1212
- 990. Some aspects of the nitration of the mononitrotoluenes. J. G. Tillett
, J. Chem. Soc.
, 1962
, 5142
- XXXIV.—The products of nitration of toluene. William Howieson Gibson, Rebecca Duckham, Ruth Fairbairn
, J. Chem. Soc., Trans.
, 1922
, 121
, 270
- Factors affecting the selectivity of the photocatalytic conversion of nitroaromatic compounds over TiO2 to valuable nitrogen-containing organic compounds. Amer Hakki, Ralf Dillert, Detlef W. Bahnemann
, Phys. Chem. Chem. Phys.
, 2013
, 15
, 2992
- Synthesis of unsaturated secondary amines by direct reductive amination of aliphatic aldehydes with nitroarenes over Au/Al2O3 catalyst in continuous flow mode. A. L. Nuzhdin, E. A. Artiukha, G. A. Bukhtiyarova, S. Yu Zaytsev, P. E. Plyusnin, Yu V. Shubin, V. I. Bukhtiyarov
, RSC Adv.
, 2016
, 6
, 88366