𝔖 Bobbio Scriptorium
✦   LIBER   ✦

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

No coin nor oath required. For personal study only.

✦ 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.


📜 SIMILAR VOLUMES


Intramolecular aromatic substitution and
✍ D. V. Ramana; M. S. Sudha 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 382 KB

## 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