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Stacking-controlled phototransformations of the 5-fluorouracil residues in dinucleotide model compounds
J J Langer1, H Wójtowicz, K Golankiewicz
1A. Mickiewicz University, Faculty of Chemistry, Poznan Poland.
Journal of Photochemistry and Photobiology. B, Biology
|October 1, 1989
Abstract:
5-Fluorouracil residues can form cyclobutane-type photodimers in a direct excitation stacking-controlled process. The stacking also has an important effect on the photohydration of uracil and 5-fluorouracil in our model compounds 5RUra(CH2)35FUra, where R = H, CH3, C2H5, C3H7, F or Cl.