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Electron‐impact induced decomposition of some 3‐alkyl‐5‐substituted‐6‐methyl uracils

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1995
Authors
Jovanović, Bratislav Ž.
Perić, A A
Vajs, Vlatka
Article (Published version)
,
John Wiley & Sons
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Abstract
Mass spectrometry was used to study the main fragmentation routes of some 3‐alkyl‐5‐substituted‐6‐methyl uracils. Differences in fragmentation were caused by changes in the structure of the alkyl group in position 3 of the uracil ring, with the same substituent in position 5, and by differences in the substituent in position 5. Copyright © 1995 John Wiley & Sons, Ltd.
Source:
Rapid Communications in Mass Spectrometry, 1995, 9, 9, 854-855
Publisher:
  • John Wiley & Sons
Projects:
  • Ministry for Science and Technology of the Republic of Serbia

DOI: 10.1002/rcm.1290090927

ISSN: 0951-4198

Scopus: 2-s2.0-85024821993
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URI
http://cer.ihtm.bg.ac.rs/handle/123456789/2797
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