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- 115. Preparation of 1 : 3-dinitronaphthalene. Herbert H. Hodgson, Stanley Birtwell
, J. Chem. Soc.
, 1943
, 433
- 30. The monoreduction of 1 : 3-dinitronaphthalene and the separation of 3-nitro-1-naphthylamine and 4-nitro-2-naphthylamine. Herbert H. Hodgson, Stanley Birtwell
, J. Chem. Soc.
, 1944
, 75
- Intermediates in nucleophilic aromatic substitution. Part XIV. Interaction of lyate ions with polynitronaphthalenes. Willie L. Hinze, Li-Jen Liu, Janos H. Fendler
, J. Chem. Soc., Perkin Trans. 2
, 1975
, 1751
- 102. The separation of 3-nitro-1-naphthylamine and 4-nitro-2-naphthylamine by maleic anhydride, and the monobromination of 4-nitro-2-naphthylamine. Herbert H. Hodgson, David E. Hathway
, J. Chem. Soc.
, 1944
, 385
- 2 : 3-Derivatives of naphthalene. Part I. The nitration of N-acetyl-3-nitro-1-naphthylamine. E. R. Ward, T. M. Coulson, J. G. Hawkins
, J. Chem. Soc.
, 1954
, 4541
- 366. Proton magnetic resonance spectra of dinitronaphthalenes. P. R. Wells
, J. Chem. Soc.
, 1963
, 1967
- Electrochemically promoted nucleophilic aromatic substitution in room temperature ionic liquids—an environmentally benign way to functionalize nitroaromatic compounds. Hugo Cruz, Iluminada Gallardo, Gonzalo Guirado
, Green Chem.
, 2011
, 13
, 2531
- Nanoparticle-based monoliths for chromatographic separations. Sheng Tang, Yong Guo, Chunming Xiong, Shujuan Liu, Xia Liu, Shengxiang Jiang
, Analyst
, 2014
, 139
, 4103
- 85. The monoreduction of dinitronaphthalenes in acid solution and of 1 : 5- and 1 : 6-dinitronaphthalene by aqueous sodium sulphide. Herbert H. Hodgson, Harold S. Turner
, J. Chem. Soc.
, 1943
, 318
- Ionic liquids as an electrolyte for the electro synthesis of organic compounds. Murugavel Kathiresan, David Velayutham
, Chem. Commun.
, 2015
, 51
, 17499