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Gold(I)-catalyzed enantioselective cycloaddition reactions
In recent years there have been extraordinary developments of gold(I)-catalyzed enantioselective processes. This includes progress in the area of cycloaddition reactions, which are of particular interest due to their potential for the rapid construction of optically active cyclic products. In this a...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Beilstein-Institut
2013
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817474/ https://www.ncbi.nlm.nih.gov/pubmed/24204438 http://dx.doi.org/10.3762/bjoc.9.264 |
| _version_ | 1782478080964558848 |
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| author | López, Fernando Mascareñas, José L |
| author_facet | López, Fernando Mascareñas, José L |
| author_sort | López, Fernando |
| collection | PubMed |
| description | In recent years there have been extraordinary developments of gold(I)-catalyzed enantioselective processes. This includes progress in the area of cycloaddition reactions, which are of particular interest due to their potential for the rapid construction of optically active cyclic products. In this article we will summarize some of the most remarkable examples, emphasizing reaction mechanisms and key intermediates involved in the processes. |
| format | Online Article Text |
| id | pubmed-3817474 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2013 |
| publisher | Beilstein-Institut |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-38174742013-11-07 Gold(I)-catalyzed enantioselective cycloaddition reactions López, Fernando Mascareñas, José L Beilstein J Org Chem Review In recent years there have been extraordinary developments of gold(I)-catalyzed enantioselective processes. This includes progress in the area of cycloaddition reactions, which are of particular interest due to their potential for the rapid construction of optically active cyclic products. In this article we will summarize some of the most remarkable examples, emphasizing reaction mechanisms and key intermediates involved in the processes. Beilstein-Institut 2013-10-30 /pmc/articles/PMC3817474/ /pubmed/24204438 http://dx.doi.org/10.3762/bjoc.9.264 Text en Copyright © 2013, López and Mascareñas 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 | Review López, Fernando Mascareñas, José L Gold(I)-catalyzed enantioselective cycloaddition reactions |
| title | Gold(I)-catalyzed enantioselective cycloaddition reactions |
| title_full | Gold(I)-catalyzed enantioselective cycloaddition reactions |
| title_fullStr | Gold(I)-catalyzed enantioselective cycloaddition reactions |
| title_full_unstemmed | Gold(I)-catalyzed enantioselective cycloaddition reactions |
| title_short | Gold(I)-catalyzed enantioselective cycloaddition reactions |
| title_sort | gold(i)-catalyzed enantioselective cycloaddition reactions |
| topic | Review |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817474/ https://www.ncbi.nlm.nih.gov/pubmed/24204438 http://dx.doi.org/10.3762/bjoc.9.264 |
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