Mass spectrometry of dinucleotide analogues containing 6‐azauracil moiety | Zendy

ZasadaParzyńska Alicja | Zendy; Golankiewicz Krzysztof | Zendy

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Mass spectrometry of dinucleotide analogues containing 6‐azauracil moiety

Author(s) -

ZasadaParzyńska Alicja,

Golankiewicz Krzysztof

Publication year - 1982

Publication title -

organic mass spectrometry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.475

H-Index - 121

eISSN - 1096-9888

pISSN - 0030-493X

DOI - 10.1002/oms.1210171205

Subject(s) - fragmentation (computing) , chemistry , moiety , phosphodiester bond , mass spectrometry , methylene , metastability , stereochemistry , medicinal chemistry , organic chemistry , chromatography , biochemistry , biology , rna , ecology , gene

The mass fragmentation of three dinucleotide analogues in which D ‐ribose phosphodiester linkages were replaced by a three methylene unit chain has been investigated. The fragmentation pathways were proposed on the basis of high resolution data and metastable transitions. These compounds demonstrated a unique fragmentation with the formation of the fragment ion containing nitrogen at the end of the C 3 H 6 chain.

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