Photochemistry and Photobiology · 1977 · 14 citations · 16 references
Natural SciencesBiochemistryMolecular BiologyBiophysical ChemistryRadiation BiophysicsRadiobiologyCellular Radiation ResponsePhotochemical SynthesisPhotochemistryRadiation ChemistryRadiation SensitivityUltraviolet Radiation BiologyIrradiation DamageIrradiation EffectsPhotosensitizersPhotosensitizing CompoundsRadiation Chemistry Of Biological MoleculesRadiation-induced Reaction MechanismsReaction Quantum YieldsUltraviolet Photochemistry
Abstract. 5,5‘‐Diuridinyl and 5,5’‐dideoxyuridinyl have been isolated from UV irradiation (254nm) in a frozen state of 5‐bromouridine and 5‐bromodeoxyuridine, respectively. These compounds were characterized by UV, IR, NMR, and mass spectra. They are formed in relatively high quantum yields which are comparable to thymidine dimerization and were found to be unaffected upon further irradiation. This photostability suggests that these 5,5‘‐coupled products, if formed, may accumulate in biological systems. Experiments carried out in “puddles” indicate, by negative inference, that the main reaction pathway is probably the recombination of two radicals to yield the coupled products in a frozen state. Therefore, the coupled products formation should be explored as a possible mechanism for the increased radiation and photosensitivity of biological systems when thymine in DNA is replaced with 5‐halouracil. In addition, these compounds may be synthesized chemically, though, in very low yields, ˜7%.
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Photochemical Reactions in Frozen Solutions
Shih Yi Wang · Nature · 1961 · 156 citations
Lipase Activity in the Brown and Yellow Adipose Tissue of the Bat
John C. George, J Eapen · Nature · 1959 · 121 citations
ORGANIC PHOTOCHEMISTRY OF NUCLEIC ACIDS*
A. Wacker, Hanswerner Dellweg, Lothar Träger et al. · Photochemistry and Photobiology · 1964 · 117 citations