Electron‐impact induced decomposition of some 3‐alkyl‐5‐substituted‐6‐methyl uracils
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1995
Article (Published version)

John Wiley & Sons
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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, 854-855Publisher:
- John Wiley & Sons
Projects:
- Ministry for Science and Technology of the Republic of Serbia