Hydrogen atom abstraction and cycloaddition-cycloreversion reactions between ionized vinylamine and neutral olefins were studied in a Fourier transform ion cyclotron resonance spectrometer. The efficiencies of both processes are appreciably less than unity. The trend in reaction efficiencies is cons
Reactivity of vinylamine radical cation with neutral dienes
โ Scribed by Guy Bouchoux; Florence Penaud-Berruyer
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 518 KB
- Volume
- 29
- Category
- Article
- ISSN
- 1076-5174
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โฆ Synopsis
Abstract
The gasโphase ionโmolecule reactions between ionized vinylamine ([CH~2~ ๏ฃพ CHNH~2~]^+.^) as a set of conjugated and unconjugated dienes were studied by Fourier transform is observed. Conjugated dienes lead to the elimination of NH~3~ or of an hydrocarbon radical from the adduct [M + CH~2~ ๏ฃพ CHNH~2~]^+.^. In the case of unconjugated dienes a regiospecific cyclobutanationโcycloreversion process is observed. Reaction mechanisms are proposed to explain these experimental findings.
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