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Gold(I)-catalyzed formation of furans from γ-acyloxyalkynyl ketones
Various γ-acyloxyalkynyl ketones were efficiently converted into highly substituted furans with 2.5 mol % of triflimide (triphenylphosphine)gold(I) as a catalyst in dichloroethane at 70 °C.
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Beilstein-Institut
2013
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3778415/ https://www.ncbi.nlm.nih.gov/pubmed/24062842 http://dx.doi.org/10.3762/bjoc.9.206 |
| _version_ | 1782285110824927232 |
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| author | Hoffmann, Marie Miaskiewicz, Solène Weibel, Jean-Marc Pale, Patrick Blanc, Aurélien |
| author_facet | Hoffmann, Marie Miaskiewicz, Solène Weibel, Jean-Marc Pale, Patrick Blanc, Aurélien |
| author_sort | Hoffmann, Marie |
| collection | PubMed |
| description | Various γ-acyloxyalkynyl ketones were efficiently converted into highly substituted furans with 2.5 mol % of triflimide (triphenylphosphine)gold(I) as a catalyst in dichloroethane at 70 °C. |
| format | Online Article Text |
| id | pubmed-3778415 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2013 |
| publisher | Beilstein-Institut |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-37784152013-09-23 Gold(I)-catalyzed formation of furans from γ-acyloxyalkynyl ketones Hoffmann, Marie Miaskiewicz, Solène Weibel, Jean-Marc Pale, Patrick Blanc, Aurélien Beilstein J Org Chem Letter Various γ-acyloxyalkynyl ketones were efficiently converted into highly substituted furans with 2.5 mol % of triflimide (triphenylphosphine)gold(I) as a catalyst in dichloroethane at 70 °C. Beilstein-Institut 2013-08-30 /pmc/articles/PMC3778415/ /pubmed/24062842 http://dx.doi.org/10.3762/bjoc.9.206 Text en Copyright © 2013, Hoffmann et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
| spellingShingle | Letter Hoffmann, Marie Miaskiewicz, Solène Weibel, Jean-Marc Pale, Patrick Blanc, Aurélien Gold(I)-catalyzed formation of furans from γ-acyloxyalkynyl ketones |
| title | Gold(I)-catalyzed formation of furans from γ-acyloxyalkynyl ketones |
| title_full | Gold(I)-catalyzed formation of furans from γ-acyloxyalkynyl ketones |
| title_fullStr | Gold(I)-catalyzed formation of furans from γ-acyloxyalkynyl ketones |
| title_full_unstemmed | Gold(I)-catalyzed formation of furans from γ-acyloxyalkynyl ketones |
| title_short | Gold(I)-catalyzed formation of furans from γ-acyloxyalkynyl ketones |
| title_sort | gold(i)-catalyzed formation of furans from γ-acyloxyalkynyl ketones |
| topic | Letter |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3778415/ https://www.ncbi.nlm.nih.gov/pubmed/24062842 http://dx.doi.org/10.3762/bjoc.9.206 |
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