Gold-catalyzed cyclization of nonterminal propargylic amides to substituted alkylideneoxazolines and -oxazines
The substrate scope of the gold-catalyzed cyclization of nonterminal propargylic amides to oxazolines and oxazines was investigated. Sixteen alkyl-substituted and 35 aryl-substited substrates were prepared by a very variable route from trimethylsilyl-(TMS-)protected, nonterminal propargylamines. Ste...
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| Hauptverfasser: | , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
22 June 2011
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| In: |
European journal of organic chemistry
Year: 2011, Heft: 24, Pages: 4595-4602 |
| ISSN: | 1099-0690 |
| DOI: | 10.1002/ejoc.201100342 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/ejoc.201100342 Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/ejoc.201100342 
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| Verfasserangaben: | A. Stephen K. Hashmi, Andreas M. Schuster, Martin Schmuck, and Frank Rominger |