Stacking-controlled phototransformations of the 5-fluorouracil residues in dinucleotide model compounds
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.
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| Published in | Journal of photochemistry and photobiology. B, Biology Vol. 4; no. 1; p. 15 |
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| Main Authors | , , |
| Format | Journal Article |
| Language | English |
| Published |
Switzerland
01.10.1989
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| 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. |
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| AbstractList | 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. |
| Author | Golankiewicz, K Wójtowicz, H Langer, J J |
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| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/2509658$$D View this record in MEDLINE/PubMed |
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| Snippet | 5-Fluorouracil residues can form cyclobutane-type photodimers in a direct excitation stacking-controlled process. The stacking also has an important effect on... |
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| SubjectTerms | Fluorouracil - radiation effects Kinetics Models, Chemical Oligoribonucleotides - radiation effects Photochemistry Ultraviolet Rays |
| Title | Stacking-controlled phototransformations of the 5-fluorouracil residues in dinucleotide model compounds |
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