Three-component synthesis of ynediones by a glyoxylation/Stephens-Castro coupling sequence
One step back, two steps forward! Starting from diverse heterocycles, the title reaction furnishes ynediones under very mild conditions in a direct and preparatively simple one-pot process. The key to avoiding decarbonylation is the CuI-catalyzed Stephens-Castro alkynylation rather than the usually...
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| Hauptverfasser: | , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
23 February 2011
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| In: |
Angewandte Chemie. International edition
Year: 2011, Jahrgang: 50, Heft: 13, Pages: 2966-2969 |
| ISSN: | 1521-3773 |
| DOI: | 10.1002/anie.201007194 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/anie.201007194 Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.201007194 |
| Verfasserangaben: | Eugen Merkul, Janis Dohe, Charlotte Gers, Frank Rominger, and Thomas J.J. Müller |
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| 520 | |a One step back, two steps forward! Starting from diverse heterocycles, the title reaction furnishes ynediones under very mild conditions in a direct and preparatively simple one-pot process. The key to avoiding decarbonylation is the CuI-catalyzed Stephens-Castro alkynylation rather than the usually more efficient Sonogashira coupling. In addition, novel highly atom-economical four-component syntheses of various heterocycles can be achieved. | ||
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