Abstract
Mercurated nucleic acids are converted to the corresponding tritiated, brominated, and iodinated derivatives by treatment with sodium borotritiide, N-bromosuccinimide, and elemental iodine, respectively. All three reactions occur under mild conditions in neutral aqueous solutions. Mercury-halogen conversions are essentially quantitative at both the mono- and polynucleotide levels. Tritiation reactions also proceed efficiently with mononucleotides, although polymers undergo incomplete demercuration. In spite of the latter limitation , these reactions provide novel and efficient synthetic routes to radiolabeled nucleic acid derivatives.
MeSH Terms
Borohydrides
Bromine
Bromosuccinimide
Cytosine Nucleotides
Iodine
Isotope Labeling/methods
Mercury
Nucleotides/analysis
Polynucleotides/analysis
Spectrophotometry, Ultraviolet
Uracil Nucleotides
Chemicals
Borohydrides
Cytosine Nucleotides
Nucleotides
Polynucleotides
Uracil Nucleotides
Iodine
Mercury
Bromosuccinimide
Bromine
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Dale R M
Ward D C
Livingston D C
Martin E
References (6)
6 references, click to expand
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