Issue 0, 1968

The alkaline degradation of deoxyribonucleic acid derivatives

Abstract

Alkaline degradation of apurinic acid and apyrimidinic acid gave, in addition to oligonucleotides and inorganic phosphate, appreciable amounts of 2-oxocyclopent-1-enyl phosphate, identical with a sample obtained by the phosphorylation of cyclopentane-1,2-dione. A mechanism for the alkaline degradation of these deoxyribonucleic acid derivatives consistent with these results and those of other workers is proposed.

Article information

Article type
Paper

J. Chem. Soc. C, 1968, 2042-2044

The alkaline degradation of deoxyribonucleic acid derivatives

A. S. Jones, A. M. Mian and R. T. Walker, J. Chem. Soc. C, 1968, 2042 DOI: 10.1039/J39680002042

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