z-logo
Premium
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.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom