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Synthetic applications of gold-catalyzed ring expansions
The development of new methodologies catalyzed by late transition metals involving cycloisomerizations of strained rings can open new venues for the synthesis of structurally complex molecules with interesting biological activities. Herein we summarize, from both a synthetic as well as a mechanistic...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3139417/ https://www.ncbi.nlm.nih.gov/pubmed/21772928 http://dx.doi.org/10.3762/bjoc.7.87 |
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author | Garayalde, David Nevado, Cristina |
author_facet | Garayalde, David Nevado, Cristina |
author_sort | Garayalde, David |
collection | PubMed |
description | The development of new methodologies catalyzed by late transition metals involving cycloisomerizations of strained rings can open new venues for the synthesis of structurally complex molecules with interesting biological activities. Herein we summarize, from both a synthetic as well as a mechanistic point of view, the most recent developments in gold-catalyzed ring expansions. |
format | Online Article Text |
id | pubmed-3139417 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-31394172011-07-19 Synthetic applications of gold-catalyzed ring expansions Garayalde, David Nevado, Cristina Beilstein J Org Chem Review The development of new methodologies catalyzed by late transition metals involving cycloisomerizations of strained rings can open new venues for the synthesis of structurally complex molecules with interesting biological activities. Herein we summarize, from both a synthetic as well as a mechanistic point of view, the most recent developments in gold-catalyzed ring expansions. Beilstein-Institut 2011-06-07 /pmc/articles/PMC3139417/ /pubmed/21772928 http://dx.doi.org/10.3762/bjoc.7.87 Text en Copyright © 2011, Garayalde and Nevado 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 Garayalde, David Nevado, Cristina Synthetic applications of gold-catalyzed ring expansions |
title | Synthetic applications of gold-catalyzed ring expansions |
title_full | Synthetic applications of gold-catalyzed ring expansions |
title_fullStr | Synthetic applications of gold-catalyzed ring expansions |
title_full_unstemmed | Synthetic applications of gold-catalyzed ring expansions |
title_short | Synthetic applications of gold-catalyzed ring expansions |
title_sort | synthetic applications of gold-catalyzed ring expansions |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3139417/ https://www.ncbi.nlm.nih.gov/pubmed/21772928 http://dx.doi.org/10.3762/bjoc.7.87 |
work_keys_str_mv | AT garayaldedavid syntheticapplicationsofgoldcatalyzedringexpansions AT nevadocristina syntheticapplicationsofgoldcatalyzedringexpansions |