Our studies have revealed reagents that can attack the 5,6-double bond of pyrimidine nucleosides; potassium permanganate and bisulfite. This review is a personal account of these studies, with a discussion on the vulnerable nature of this particular double bond to external nucleophiles and oxidizing agents. The finding that N(4)aminocytidine, produced on treatment of cytidine with bisulfite and hydrazine, is a strong mutagen is also described.
CITATION STYLE
Hayatsu, H. (1996). The 5,6-double bond of pyrimidine nucleosides, a fragile site in nucleic acids. Journal of Biochemistry. Oxford University Press. https://doi.org/10.1093/oxfordjournals.jbchem.a021253
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