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- Organic dye-photocatalyzed fluoroalkylation of heteroarene-N-oxide derivatives. Beatriz Lantaño, Sebastián Barata-Vallejo, Al Postigo
, Org. Biomol. Chem.
, 2018
, 16
, 6718
- Chlorine-35 nuclear quadrupole resonance study of molecular torsional motion in some chloropyridine-N-oxides and chloroquinoline-N-oxides. P. S. Raghoottama, S. Soundararajan, J. Ramakrishna
, J. Chem. Soc., Faraday Trans. 2
, 1989
, 85
, 131
- Regiospecific thermal rearrangements of 2-allyloxypyridine N-oxides. David Alker, Sivapathasuntharam Mageswaran, W. David Ollis, Hooshang Shahriari-Zavareh
, J. Chem. Soc., Perkin Trans. 1
, 1990
, 1631
- Periselectivity between the [1,4] and [3,3] thermal sigmatropic rearrangements of 2-allyloxypyridine N-oxides. David Alker, W. David Ollis, Hooshang Shahriari-Zavareh
, J. Chem. Soc., Perkin Trans. 1
, 1990
, 1623
- Recyclable anhydride catalyst for H2O2 oxidation: N-oxidation of pyridine derivatives. Ghellyn Gajeles, Se Mi Kim, Jong-Cheol Yoo, Kyung-Koo Lee, Sang Hee Lee
, RSC Adv.
, 2020
, 10
, 9165
- Computationally designed tandem direct selective oxidation using molecular oxygen as oxidant without coreductant. Bo Yang, Thomas A. Manz
, RSC Adv.
, 2016
, 6
, 88189
- Evaluation of the polar–inductive and mesomeric effects exerted on contiguous functionalities by N-oxidopyridinium groups. Emma Barchiesi, Silvia Bradamante, Carla Carfagna, Raffaella Ferraccioli, Giorgio A. Pagani
, J. Chem. Soc., Perkin Trans. 2
, 1987
, 1009
- 875. N-oxides and related compounds. Part V. The tautomerism of 2- and 4-amino- and -hydroxy-pyridine 1-oxide. J. N. Gardner, A. R. Katritzky
, J. Chem. Soc.
, 1957
, 4375
- FTIR investigation of O···H···O hydrogen bonds with large proton polarizability in sulfonic acid–N-oxide systems in the middle and far-IR. Roland Langner, Georg Zundel
, J. Chem. Soc., Faraday Trans.
, 1998
, 94
, 1805
- Aromatic substitution. Part XVIII. Kinetics of reactions between some halogeno-pyridines and -picolines and their N-oxides with methoxide ion in methanol and in dimethyl sulphoxide. Effect of alkyl groups on rates on orientation in nucleophilic aromatic substitution. R. A. Abramovitch, F. Helmer, M. Liveris
, J. Chem. Soc. B
, 1968
, 492