Ring-closing olefin metathesis in the aqueous phase of amphiphilic conetworks consisting of fluorophilic and hydrophilic compartments
EM Hensle, J Tobis, JC Tiller, W Bannwarth
Index: Hensle, Eva M.; Tobis, Jan; Tiller, Joerg C.; Bannwarth, Willi Journal of Fluorine Chemistry, 2008 , vol. 129, # 10 p. 968 - 973
Full Text: HTML
Citation Number: 30
Abstract
A Grubbs–Hoveyda-Type metathesis catalyst bearing a tris (perfluoroalkyl) silyl tag was immobilized in the fluorophilic phase of amphiphilic conetworks (APCNs). This catalytic system was applied to ring-closing metathesis (RCM) reactions in aqueous media. Different substrates were evaluated and with 10mol% of catalyst at 60° C good conversions were observed. Reuse of the catalytic system was possible, but resulted generally in lower ...
Related Articles:
Catalytic deallylation of allyl-and diallylmalonates
[Necas, David; Tursky, Matyas; Kotora, Martin Journal of the American Chemical Society, 2004 , vol. 126, # 33 p. 10222 - 10223]