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- Alkyl bromide photobromination: catalysis by hydrogen bromide and the elimination–readdition pathway. Jean-Ph. Soumillion, Claude Ronneau, Pierre Dejaifve
, J. Chem. Soc., Perkin Trans. 2
, 1983
, 1907
- A novel amino acid analysis method using derivatization of multiple functional groups followed by liquid chromatography/tandem mass spectrometry. Yohei Sakaguchi, Tomoya Kinumi, Taichi Yamazaki, Akiko Takatsu
, Analyst
, 2015
, 140
, 1965
- 65. A criterion for the mechanism of the reaction between alkyl halides and hydroxylic solvents. Part III. Reactions of n-butyl bromide. Marjorie L. Bird, Edward D. Hughes, Christopher K. Ingold
, J. Chem. Soc.
, 1943
, 255
- Liquid-phase bromination of bromobutane: variation of the ratio of 1,2- to 1,3-dibromobutanes produced. Keith Ody, Antony Nechvatal, John M. Tedder
, J. Chem. Soc., Perkin Trans. 2
, 1976
, 521
- 180. Mechanism of substitution at a saturated carbon atom. Part XV. Unimolecular and bimolecular substitutions of n-butyl bromide with water, and with anions, as substituting agents in formic acid solution. Leslie C. Bateman, Edward D. Hughes
, J. Chem. Soc.
, 1940
, 940
- Kinetics of quaternization of 4-methyl and 4-ethyl pyridine with n-propyl and n-butyl bromide in sulpholane. Ernest A. Boucher, Ezatollah Khosravi-Babadi, Christopher C. Mollett
, J. Chem. Soc., Faraday Trans. 1
, 1978
, 74
, 427
- Empirical correlations of partial molar volumes at infinite dilution of organic solutes and transition states for S
N
2 hydrolysis and ethanolysis of n-alkyl bromides. Hidenori Itsuki, Mikizo Kuwabara, Kouji Hayase, Seiji Terasawa
, J. Chem. Soc., Perkin Trans. 2
, 1989
, 563
- Imidazolium modified carbon nanohorns: switchable solubility and stabilization of metal nanoparticles. Nikolaos Karousis, Toshinari Ichihashi, Shimou Chen, Hisanori Shinohara, Masako Yudasaka, Sumio Iijima, Nikos Tagmatarchis
, J. Mater. Chem.
, 2010
, 20
, 2959
- Studies of olefin formation in the pyrolysis of n-butyl bromide. M. R. Bridge, J. L. Holmes
, J. Chem. Soc. B
, 1967
, 1008
- Isoleucine ionic liquids as additives to separate mandelic acid and their derivative enantiomers by HPLC. Jie Zhou, Suzhen Zhao, Guangjun Fu, Zhenzhong Zhang
, Anal. Methods
, 2014
, 6
, 5627