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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...

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Detalles Bibliográficos
Autores principales: Sarria Toro, Juan M., García‐Morales, Cristina, Raducan, Mihai, Smirnova, Ekaterina S., Echavarren, Antonio M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
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.
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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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