## Abstract __N__(Pyrimidin‐2‐yl)‐glycine, ‐alanine and ‐phenylalanine (1‐3) and their methyl esters (4‐6) were investigated using electron impact (EI) mass Spectrometry. The results showed that EI‐induced decomposition occurs on the carboxylic group or involves the loss of R~2~OH. In contrast to e
Ortho effect in the mass spectrometric behaviour of N(pyrimidin-4-yl)aminobenzoic acids and their methyl esters
✍ Scribed by Adam S. Plaziak; Jaroslaw Spychala; Hanna Wójtowicz; Jerzy J. Langer; Halina Thiel-Pawlicka; Krzysztof Golankiewicz
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 410 KB
- Volume
- 27
- Category
- Article
- ISSN
- 1076-5174
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✦ Synopsis
Ortho-, meta-and para-isomers of N-(pyrimidin-4-yl)aminobenzoic acid and their methyl esters were investigated by electron impact mass spectrometry. Their fragmentation was found to be strongly dependent on the position of the substituent in the aminobenzoic moiety. Two different kinds of ortho effect were studied and confirmed with the aid of deuterium-labelled derivatives.
📜 SIMILAR VOLUMES
## Abstract Photoionisation mass spectra of __N__‐methylamides of __N__‐acetyl derivatives of the following amino acids have been studied: alanine, valine, leucine, serine, threonine, phenylalanine, tyrosine, tryptophan and proline. The study also included methyl esters of __N__‐acetyl tyrosine, __