Journal
ORGANIC LETTERS
Volume 17, Issue 2, Pages 246-249Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol5033267
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Funding
- French Agence National pour la Recherche through the DNAExciton project [ANR-10-BLAN-0809]
- French Agence National pour la Recherche through the OPHID project [ANR-12-BS08-0001-02]
- Agence Nationale de la Recherche (ANR) [ANR-10-BLAN-0809] Funding Source: Agence Nationale de la Recherche (ANR)
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Structural features are of major importance for the formation of mutagenic photoproducts in DNA. It was recently reported that lack of constraints between two adjacent nucleosidic units prevents the conversion of pyrimidine (64) pyrimidone photoproducts into their Dewar valence isomers. We here report that this is not the case for the thymidine photoproducts which, although unconstrained, are quantitatively converted into photolysis products identified as Dewar valence isomers by mass spectrometry and NMR and infrared spectroscopies.
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