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120Osama K. Abou-Zied and Othman I. K. Al-Shihi.
Caging and solvent effects on the tautomeric equilibrium of 3-pyridone/3-hydroxypyridine in the ground state: a study in cyclodextrins and binary solvents, Phys. Chem. Chem. Phys., 2009, 11, 5377. Tae-gyu Nam, Susheel J. Nara, Irène Zagol-Ikapitte, Thomas Cooper, Luca Valgimigli, John A. Oates, Ned A. Porter, Olivier Boutaud and Derek A. Pratt.
Pyridine and pyrimidine analogs of acetaminophen as inhibitors of lipid peroxidation and cyclooxygenase and lipoxygenase catalysis, Org. Biomol. Chem., 2009, 7, 5103. María C. Gutiérrez, Daniel Carriazo, Conchi O. Ania, Jose B. Parra, M. Luisa Ferrer and Francisco del Monte.
Deep eutectic solvents as both precursors and structure directing agents in the synthesis of nitrogen doped hierarchical carbons highly suitable for CO2 capture, Energy Environ. Sci., 2011, 4, 3535. Luigi Anastasia, Mario Anastasia and Pietro Allevi.
A practical protocol for the synthesis of 3-hydroxy-4,5-disubstituted pyridine derivatives from acyclic compounds, J. Chem. Soc., Perkin Trans. 1, 2001, 0, 2404. José Natera, Walter Massad and Norman A. García.
The role of vitamin B6 as an antioxidant in the presence of vitamin B2-photogenerated reactive oxygen species. A kinetic and mechanistic study, Photochem. Photobiol. Sci., 2012, 11, 938. Miquel Adrover, Catalina Caldés, Bartolomé Vilanova, Juan Frau, Josefa Donoso and Francisco Muñoz.
Towards a detailed description of pyridoxamine tautomeric species, New J. Chem., 2012, 36, 1751. Mahmut Durmus and Tebello Nyokong.
Synthesis, photophysical and photochemical studies of new water-soluble indium(iii) phthalocyanines, Photochem. Photobiol. Sci., 2007, 6, 659. Role of the GABA-benzodiazepine-receptor complex in the mechanism of the anxtolytic action of 3-hydroxypyridines u2014 New tranquilizers with a nonbenzodiazepine structure, Bulletin of Experimental Biology and Medicine Catalysis in ??-elimination reactions, Bulletin of the Academy of Sciences of the USSR, Division of chemical science Study of basic deuterium exchange in series of 4-hydroxyisoquinoline, 3-hydroxyquinoline, and 8-hydroxyquinoline derivatives, Bulletin of the Academy of Sciences of the USSR, Division of chemical science