Mechanistic investigation of the isomerization of 5-vinyl-2-norbornene

Authors
Kim, HSLee, SYLee, HBae, JYPark, SJCheong, MLee, JSLee, CH
Issue Date
2006-02-03
Publisher
AMER CHEMICAL SOC
Citation
JOURNAL OF ORGANIC CHEMISTRY, v.71, no.3, pp.911 - 914
Abstract
The isomerization reaction of 5-vinyl-2-norbornene (VNB) to 5-ethylidene-2-norbornene (ENB) has been performed using a catalytic system consisting of an alkali metal hydride and an amine. Among various amines tested, only aliphatic 1,2-diamines exhibited the activity for the isomerization. The isomerization was also affected by the alkali metal hydride employed. The activity of the alkali metal hydride increased with the increasing size of alkali metal: KH > NaH > LiH. A series of electron paramagnetic resonance (EPR) and UV-vis experiments on the active species suggest that the isomerization of VNB proceeds through a radical mechanism.
Keywords
4N/5E RADICAL-ANIONS; ELECTRON DELOCALIZATION; 4N/6E DIANIONS; 4N/5E RADICAL-ANIONS; ELECTRON DELOCALIZATION; 4N/6E DIANIONS
ISSN
0022-3263
URI
https://pubs.kist.re.kr/handle/201004/135755
DOI
10.1021/jo0518203
Appears in Collections:
KIST Article > 2006
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