𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Electron impact-induced rearrangement of trimethylsilyl groups in long chain compounds

✍ Scribed by G. H. Draffan; R. N. Stillwell; James A. McCloskey

Publisher
John Wiley and Sons
Year
1968
Tongue
English
Weight
819 KB
Volume
1
Category
Article
ISSN
1076-5174

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

A McLafferty-type rearrangement of a tri
A McLafferty-type rearrangement of a trimethylsilyl group in silylated hydroxy carbonyl compounds
✍ G. Petersson πŸ“‚ Article πŸ“… 1972 πŸ› John Wiley and Sons 🌐 English βš– 908 KB

A McLafferty-type rearrangement of a trimethylsilyl group is demonstrated. Abundant rearrangement ions are formed for trimethylsilyl derivatives of cc,p-dihydroxy carbonyl compounds. Data are given for a large number of hydroxy acids and hydroxy ketones including aldonic acids, aldaric acids, acycli

Thermally and electron-impact-induced re
Thermally and electron-impact-induced rearrangements of dimethylthioncarbamates in gaseous phase
✍ James C. Tou; R. M. Rodia πŸ“‚ Article πŸ“… 1972 πŸ› John Wiley and Sons 🌐 English βš– 427 KB

The thermally and electron-impact-induced rearrangements of the dimethylthioncarbamates to the dimethylthiolcarbamates are discussed. Owing to the competition with the ion fragmentation reactions in the mass spectrometric time, seconds, the extent of the mass spectrometrically observed ion isomeriza

Substituent effect and rearrangements in
Substituent effect and rearrangements in the electron-impact spectra of long chain esters of m-and p-methoxybenzoic acid
✍ Mitchell A. Winnik; P. Y. Y. Kwong πŸ“‚ Article πŸ“… 1975 πŸ› John Wiley and Sons 🌐 English βš– 440 KB

## Abstract The mass spectra of eighteen n‐alkyl estars of p‐methoxybenzoic acid are examined. Few differences exist in the spectra of the corresponding para and meta isomers. We describe a new rearrangement, loss of OH from the molecular ion, whichis observed only in the para substituted isomkers.