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C-Arylation reactions catalyzed by CuO-nanoparticles under ligand free conditions
CuO-nanoparticles were found to be an excellent heterogeneous catalyst for C-arylation of active methylene compounds using various aryl halides. The products were obtained in good to excellent yield. The catalyst can be recovered and reused for four cycles with almost no loss in activity.
| Autores principales: | , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Beilstein-Institut
2010
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2874413/ https://www.ncbi.nlm.nih.gov/pubmed/20502607 http://dx.doi.org/10.3762/bjoc.6.35 |
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| author | Kidwai, Mazaahir Bhardwaj, Saurav Poddar, Roona |
| author_facet | Kidwai, Mazaahir Bhardwaj, Saurav Poddar, Roona |
| author_sort | Kidwai, Mazaahir |
| collection | PubMed |
| description | CuO-nanoparticles were found to be an excellent heterogeneous catalyst for C-arylation of active methylene compounds using various aryl halides. The products were obtained in good to excellent yield. The catalyst can be recovered and reused for four cycles with almost no loss in activity. |
| format | Text |
| id | pubmed-2874413 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2010 |
| publisher | Beilstein-Institut |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-28744132010-05-25 C-Arylation reactions catalyzed by CuO-nanoparticles under ligand free conditions Kidwai, Mazaahir Bhardwaj, Saurav Poddar, Roona Beilstein J Org Chem Full Research Paper CuO-nanoparticles were found to be an excellent heterogeneous catalyst for C-arylation of active methylene compounds using various aryl halides. The products were obtained in good to excellent yield. The catalyst can be recovered and reused for four cycles with almost no loss in activity. Beilstein-Institut 2010-04-15 /pmc/articles/PMC2874413/ /pubmed/20502607 http://dx.doi.org/10.3762/bjoc.6.35 Text en Copyright © 2010, Kidwai 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 | Full Research Paper Kidwai, Mazaahir Bhardwaj, Saurav Poddar, Roona C-Arylation reactions catalyzed by CuO-nanoparticles under ligand free conditions |
| title | C-Arylation reactions catalyzed by CuO-nanoparticles under ligand free conditions |
| title_full | C-Arylation reactions catalyzed by CuO-nanoparticles under ligand free conditions |
| title_fullStr | C-Arylation reactions catalyzed by CuO-nanoparticles under ligand free conditions |
| title_full_unstemmed | C-Arylation reactions catalyzed by CuO-nanoparticles under ligand free conditions |
| title_short | C-Arylation reactions catalyzed by CuO-nanoparticles under ligand free conditions |
| title_sort | c-arylation reactions catalyzed by cuo-nanoparticles under ligand free conditions |
| topic | Full Research Paper |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2874413/ https://www.ncbi.nlm.nih.gov/pubmed/20502607 http://dx.doi.org/10.3762/bjoc.6.35 |
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