Gold catalysis: domino reaction of en-diynes to highly substituted phenols
By Sonogashira coupling of 1,7-heptadiynes and 1,8-octadiynes with 2-iodoallyl alcohols, various substrates that bear a 2-alkynylallyl alcohol moiety tethered to an additional alkyne were prepared in one step. Subjection to nitrogen acyclic carbene (NAC)/gold(I) catalysts delivered highly substitute...
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| Autori principali: | , , , |
|---|---|
| Natura: | Article (Journal) |
| Lingua: | inglese |
| Pubblicazione: |
07 June 2011
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| In: |
Chemistry - a European journal
Year: 2011, Volume: 17, Fascicolo: 29, Pages: 8195-8201 |
| ISSN: | 1521-3765 |
| DOI: | 10.1002/chem.201100305 |
| Accesso online: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/chem.201100305 Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/chem.201100305 |
| Note sull'autore: | A. Stephen K. Hashmi, Tobias Häffner, Matthias Rudolph, and Frank Rominger |
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