Abstract
Three different methods that use a single ruthenium catalyst to enable the facile formation of meta- and para-substituted alkenylarenes have now been developed. The reactions proceed through a tandem alkenylation/decarboxylation process and provide several advantages over alternative approaches.
| Original language | English |
|---|---|
| Pages (from-to) | 1086-1088 |
| Number of pages | 3 |
| Journal | Nature Chemistry |
| Volume | 8 |
| Issue number | 12 |
| DOIs | |
| Publication status | Published - 22 Nov 2016 |
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