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- Acylarylnitrosamines. Part III. Decomposition of 2,5-di-(N-nitrosoacetamido)-1,4-di-t-butylbenzene and related compounds. J. I. G. Cadogan, M. J. P. Harger, J. T. Sharp
, J. Chem. Soc. B
, 1971
, 602
- Amine oxidation and the chemistry of quinone imines. Part I. 3-Methoxy-4-t-butylaniline. R. K. Haynes, F. R. Hewgill
, J. Chem. Soc., Perkin Trans. 1
, 1972
, 396
- Stepwise dissolution and composition determination of samples of multiple crystals using a dissolution medium containing aqueous alcohol and fluorocarbon phases. Humphrey A. Moynihan, Declan Armstrong
, RSC Adv.
, 2019
, 9
, 21405
- 774. The kinetics and mechanisms of aromatic halogen substitution. Part XVI. Rates and products of chlorination of biphenyl and some t-butyl-substituted biphenyls in acetic acid. P. B. D. de la Mare, E. A. Johnson
, J. Chem. Soc.
, 1963
, 4076
- Simple chip-based interfaces for on-line monitoring of supramolecular interactions by nano-ESI MS. Monica Brivio, R. Edwin Oosterbroek, Willem Verboom, Albert van den Berg, David N. Reinhoudt
, Lab Chip
, 2005
, 5
, 1111
- Derivatives of m-di-t-butylbenzene. Part 8. Dissociation constants of 2-halogeno-4,6-di-t-butylanilines, and 1H nuclear magnetic resonance spectra of the corresponding acetanilides. Adrianus Jan de Koning
, J. Chem. Soc., Perkin Trans. 2
, 1984
, 341
- Red/green-light emission in continuous dielectric phase transition materials: [Me3NVinyl]2[MnX4] (X = Cl, Br). Yanyan Li, Liting Lin, Jie Yang, Kun Qian, Tao Jiang, Hong Li
, RSC Adv.
, 2021
, 11
, 2329
- 47. Aromatic reactivity. Part XIII. Effects of methyl and t-butyl groups in aromatic detritiation. C. Eaborn, R. Taylor
, J. Chem. Soc.
, 1961
, 247
- Novel neutral hexacoordinate silicon(iv) complexes with two bidentate monoanionic benzamidinato ligands. Konstantin Junold, Christian Burschka, RĂ¼diger Bertermann, Reinhold Tacke
, Dalton Trans.
, 2010
, 39
, 9401
- Homolytic aromatic substitution. Part VII. Partial rate factors for the phenylation of tert.-butylbenzene and p-di-tert.-butylbenzene. J. I. G. Cadogan, D. H. Hey, Gareth H. Williams
, J. Chem. Soc.
, 1954
, 3352