Beilstein J. Org. Chem.2013,9, 49–55, doi:10.3762/bjoc.9.6
Satyajit Haldar Subratanath Koner Department of Chemistry, Jadavpur University, Kolkata 700032, India 10.3762/bjoc.9.6 Abstract The addition of phenols to aryl-substituted alkynes to form 1,1-diarylalkenes was carried out by using the Fe-Al-MCM-41 catalyst. The catalyst showed remarkable
improvement in time and yield in comparison to other solid catalysts. The heterogeneous catalyst can be reused at least three times without a significant loss in activity.
Keywords: 1,1-diarylalkenes; heterogeneous catalysis; Fe-Al-MCM-41; Introduction
The direct vinylation of phenols has received
made their employment an attractive choice. Recently, we have successfully employed a Fe-Al-MCM-41 catalyst in a Friedel–Crafts-type hydroarylation reaction of styrenes [33]. The catalyst demonstrated high yields of products with good selectivities within a short reaction time under “open flask
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Graphical Abstract
Figure 1:
(RS)-Tolterodine, an important urological drug.