Abstract:
Photoinduced proton transfer in crystalline 5-fluorouracil results in oxo–hydroxo tautomeric forms.
Document Type:
Article
Language: English
Citation:
S. S. Ostakhov, M. V. Sultanbaev, “Photoinduced oxo–hydroxo tautomerisation of crystalline 5-fluorouracil”, Mendeleev Commun., 22:1 (2012), 23–24
Linking options:
https://www.mathnet.ru/eng/mendc2724
https://www.mathnet.ru/eng/mendc/v22/i1/p23
This publication is cited in the following 4 articles:
S. S. Ostakhov, G. S. Abdrakhimova, R. R. Kayumova, S. P. Ivanov, S. L. Khursan, “Spectral–Luminescent and Spectrophotometric Study of Molecular and Anionic Forms of N-Methyl Derivatives of 5-Fluorouracil in Aqueous Solutions”, High Energy Chem, 56:3 (2022), 158
Sergey P. Ivanov, Sergei S. Ostakhov, Gulnaz S. Abdrakhimova, Aidar A. Akhiyarov, Sergey L. Khursan, “On the use of the spectral luminescent method for studying acid–base equilibria of uracil derivatives in aqueous solutions”, Biophysical Chemistry, 266 (2020), 106432
S. S. Ostakhov, M. Yu. Ovchinnikov, G. A. Masyagutova, S. L. Khursan, “Luminescent and DFT Study of Keto–Enol Tautomers of 5-Fluorouracil and Its Derivatives in Aqueous Solutions”, J. Phys. Chem. A, 123:37 (2019), 7956
S. S. Ostakhov, M. V. Sultanbaev, S. L. Khursan, N. M. Shishlov, Yu. A. Lebedev, R. R. Kinzyabulatov, “Photophysics and photochemistry of crystalline 5-fluorouracil”, High Energy Chem, 48:5 (2014), 330
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