Results
1 -
6 of
6
(Click
here to explore results)
- The mechanism of the electrophilic substitution of heteroaromatic compounds. Part VII. The nitration of pyridines in the α-position and rules for the nitration of substituted pyridines. C. D. Johnson, A. R. Katritzky, M. Viney
, J. Chem. Soc. B
, 1967
, 1211
- The mechanism of the electrophilic substitution of heteroaromatic compounds. Part VIII. The α-, β-, and γ-nitration of pyridine 1-oxides. C. D. Johnson, A. R. Katritzky, Naeem Shakir, M. Viney
, J. Chem. Soc. B
, 1967
, 1213
- The mechanism of the electrophilic substitution of heteroaromatic compounds. Part X. Acid-catalysed hydrogen exchange at the α-, β-, and γ-positions of substituted pyridine 1-oxides. G. P. Bean, P. J. Brignell, C. D. Johnson, A. R. Katritzky, B. J. Ridgewell, H. O. Tarhan, A. M. White
, J. Chem. Soc. B
, 1967
, 1222
- Polyhalogenated heterocyclic compounds. Part 42.1 Fluorinated nitrogen heterocycles with unusual substitution patterns. Richard D. Chambers, Christopher W. Hall, John Hutchinson, Ross W. Millar
, J. Chem. Soc., Perkin Trans. 1
, 1998
, 1705
- Nucleophilic amination of methoxypyridines by a sodium hydride–iodide composite. Jia Hao Pang, Atsushi Kaga, Shunsuke Chiba
, Chem. Commun.
, 2018
, 54
, 10324
- Asymmetric synthesis of (+)-castanospermine through enol ether metathesis–hydroboration/oxidation. Julien Ceccon, Grégory Danoun, Andrew E. Greene, Jean-François Poisson
, Org. Biomol. Chem.
, 2009
, 7
, 2029