## Abstract __N__‐(2‐Propynyl)anilines undergo amino‐Claisen rearrangement to a minor extent in the ion source, losing a molecule of HCN under electron impact conditions. However, metastable molecular ions with energies closer to threshold undergo Claisen rearrangement giving rise to more abundant
Unusual neutral and radical losses in 2′-substituted N-phenylanthranilic acids on electron impact
✍ Scribed by D. V. Ramana; R. Srinivas; P. Mahalakshmi
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 424 KB
- Volume
- 26
- Category
- Article
- ISSN
- 1076-5174
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✦ Synopsis
Abstract
Unusual expulsions of [H~2~O + CO~2~] from the M^+^˙ of N‐(o‐carboxyphenyl)anthranilic acid, [H~2~O + CH~2~O] from the M^+^˙ of N‐(o‐methoxyphenyl)anthranilic acid and [H~2~O + ˙NO~2~] from the M^+^˙ of N‐(o‐nitrophenyl) anthranilic acid were observed under electron impact conditions. These processes are stepwise in the corresponding para‐substituted N‐phenylanthranilic acids. The proposed fragmentation pathways and their mechanisms are supported by B/E linked‐scan spectra, collision‐activated decomposition (CAD)–mass‐analysed ion kinetic energy (MIKE) spectra, high‐resolution data, deuterium labelling and chemical substitution.
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