Abstract
General direct C2-alkenylation of oxazoles is reported using alkenyl tosylates at parts per million levels of palladium catalyst. From a series of ligands screened, PhMezole-Phos emerged as the promising ligand candidate to facilitate this reaction. Significantly, the method is scalable and exhibits excellent substrate tolerance. Highly sterically hindered substrates and small vinyl tosylate can be coupled successfully. Moreover, our method enables a rapid diversification of oxazole-based C^N ligands which can be readily derived into new group 9 organometallic compounds. © 2016 American Chemical Society.
| Original language | English |
|---|---|
| Pages (from-to) | 5300-5303 |
| Number of pages | 4 |
| Journal | Organic Letters |
| Volume | 18 |
| Issue number | 20 |
| Online published | 11 Oct 2016 |
| DOIs | |
| Publication status | Published - 21 Oct 2016 |
| Externally published | Yes |
Funding
We thank the Research Grants Council of Hong Kong (CRF: C5023-14G), General Research Fund (PolyU 153034/15P), and State Key Laboratory of Chirosciences for financial support.
RGC Funding Information
- RGC-funded
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