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PMID: 1144066 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Conversion of covalently mercurated nucleic acids to tritiated and halogenated derivatives.

Nucleic acids research ·Vol. 2 ·No. 6 ·1975-06-00 ·Pages 915-30

Dale RM, Ward DC, Livingston DC, Martin E

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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Article Info
Journal
Nucleic acids research
Abbr.
Nucleic Acids Res
ISSN
0305-1048
Published
1975-06-00
Pages
915-30
Language
English
Region
England
NLM ID
0411011
PMCID
PMC343478
Subset
IM
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