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Gold(I) Carbenoids: On‐Demand Access to Gold(I) Carbenes in Solution
Chloromethylgold(I) complexes of phosphine, phosphite, and N‐heterocyclic carbene ligands are easily synthesized by reaction of trimethylsilyldiazomethane with the corresponding gold chloride precursors. Activation of these gold(I) carbenoids with a variety of chloride scavengers promotes reactivity...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324612/ https://www.ncbi.nlm.nih.gov/pubmed/28090747 http://dx.doi.org/10.1002/anie.201611705 |
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author | Sarria Toro, Juan M. García‐Morales, Cristina Raducan, Mihai Smirnova, Ekaterina S. Echavarren, Antonio M. |
author_facet | Sarria Toro, Juan M. García‐Morales, Cristina Raducan, Mihai Smirnova, Ekaterina S. Echavarren, Antonio M. |
author_sort | Sarria Toro, Juan M. |
collection | PubMed |
description | Chloromethylgold(I) complexes of phosphine, phosphite, and N‐heterocyclic carbene ligands are easily synthesized by reaction of trimethylsilyldiazomethane with the corresponding gold chloride precursors. Activation of these gold(I) carbenoids with a variety of chloride scavengers promotes reactivity typical of metallocarbenes in solution, namely homocoupling to ethylene, olefin cyclopropanation, and Buchner ring expansion of benzene. |
format | Online Article Text |
id | pubmed-5324612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53246122017-03-08 Gold(I) Carbenoids: On‐Demand Access to Gold(I) Carbenes in Solution Sarria Toro, Juan M. García‐Morales, Cristina Raducan, Mihai Smirnova, Ekaterina S. Echavarren, Antonio M. Angew Chem Int Ed Engl Communications Chloromethylgold(I) complexes of phosphine, phosphite, and N‐heterocyclic carbene ligands are easily synthesized by reaction of trimethylsilyldiazomethane with the corresponding gold chloride precursors. Activation of these gold(I) carbenoids with a variety of chloride scavengers promotes reactivity typical of metallocarbenes in solution, namely homocoupling to ethylene, olefin cyclopropanation, and Buchner ring expansion of benzene. John Wiley and Sons Inc. 2017-01-16 2017-02-06 /pmc/articles/PMC5324612/ /pubmed/28090747 http://dx.doi.org/10.1002/anie.201611705 Text en © 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Communications Sarria Toro, Juan M. García‐Morales, Cristina Raducan, Mihai Smirnova, Ekaterina S. Echavarren, Antonio M. Gold(I) Carbenoids: On‐Demand Access to Gold(I) Carbenes in Solution |
title | Gold(I) Carbenoids: On‐Demand Access to Gold(I) Carbenes in Solution |
title_full | Gold(I) Carbenoids: On‐Demand Access to Gold(I) Carbenes in Solution |
title_fullStr | Gold(I) Carbenoids: On‐Demand Access to Gold(I) Carbenes in Solution |
title_full_unstemmed | Gold(I) Carbenoids: On‐Demand Access to Gold(I) Carbenes in Solution |
title_short | Gold(I) Carbenoids: On‐Demand Access to Gold(I) Carbenes in Solution |
title_sort | gold(i) carbenoids: on‐demand access to gold(i) carbenes in solution |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324612/ https://www.ncbi.nlm.nih.gov/pubmed/28090747 http://dx.doi.org/10.1002/anie.201611705 |
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