Gold(I)-catalyzed enantioselective cycloaddition reactions
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| Title: | Gold(I)-catalyzed enantioselective cycloaddition reactions |
| Author: | López García, Fernando Mascareñas Cid, José Luis |
| Affiliation: | Universidade de Santiago de Compostela. Centro de Investigación en Química Biolóxica e Materiais Moleculares Universidade de Santiago de Compostela. Departamento de Química Orgánica |
| Subject: | Alkyne | Allene | Asymmetric catalysis | Cycloaddition | Enantioselective | Gold | Gold catalysis | |
| Date of Issue: | 2013 |
| Publisher: | Beilstein-Institut |
| Citation: | López, F.; Mascareñas, J. L. Beilstein J. Org. Chem. 2013, 9, 2250–2264. doi:10.3762/bjoc.9.264 |
| Abstract: | 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 |
| Publisher version: | https://doi.org/10.3762/bjoc.9.264 |
| URI: | http://hdl.handle.net/10347/18476 |
| DOI: | 10.3762/bjoc.9.264 |
| E-ISSN: | 1860-5397 |
| Rights: | © 2013 López and Mascareñas; licensee Beilstein-Institut. This is an Open Access article under the terms of the Creative Commons Attribution License (http://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: (http://www.beilstein-journals.org/bjoc) |
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Except where otherwise noted, this item's license is described as © 2013 López and Mascareñas; licensee Beilstein-Institut. This is an Open Access article under the terms of the Creative Commons Attribution License (http://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: (http://www.beilstein-journals.org/bjoc)