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Reversible Reductive Elimination in Aluminum(II) Dihydrides
Oxidative addition and reductive elimination are defining reactions of transition‐metal organometallic chemistry. In main‐group chemistry, oxidative addition is now well‐established but reductive elimination reactions are not yet general in the same way. Herein, we report dihydrodialanes supported b...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7894477/ https://www.ncbi.nlm.nih.gov/pubmed/33022874 http://dx.doi.org/10.1002/anie.202011418 |
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author | Falconer, Rosalyn L. Nichol, Gary S. Smolyar, Ivan V. Cockroft, Scott L. Cowley, Michael J. |
author_facet | Falconer, Rosalyn L. Nichol, Gary S. Smolyar, Ivan V. Cockroft, Scott L. Cowley, Michael J. |
author_sort | Falconer, Rosalyn L. |
collection | PubMed |
description | Oxidative addition and reductive elimination are defining reactions of transition‐metal organometallic chemistry. In main‐group chemistry, oxidative addition is now well‐established but reductive elimination reactions are not yet general in the same way. Herein, we report dihydrodialanes supported by amidophosphine ligands. The ligand serves as a stereochemical reporter for reversible reductive elimination/oxidative addition chemistry involving Al(I) and Al(III) intermediates. |
format | Online Article Text |
id | pubmed-7894477 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78944772021-03-02 Reversible Reductive Elimination in Aluminum(II) Dihydrides Falconer, Rosalyn L. Nichol, Gary S. Smolyar, Ivan V. Cockroft, Scott L. Cowley, Michael J. Angew Chem Int Ed Engl Communications Oxidative addition and reductive elimination are defining reactions of transition‐metal organometallic chemistry. In main‐group chemistry, oxidative addition is now well‐established but reductive elimination reactions are not yet general in the same way. Herein, we report dihydrodialanes supported by amidophosphine ligands. The ligand serves as a stereochemical reporter for reversible reductive elimination/oxidative addition chemistry involving Al(I) and Al(III) intermediates. John Wiley and Sons Inc. 2020-11-24 2021-01-25 /pmc/articles/PMC7894477/ /pubmed/33022874 http://dx.doi.org/10.1002/anie.202011418 Text en © 2020 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH This is an open access article under the terms of the 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 Falconer, Rosalyn L. Nichol, Gary S. Smolyar, Ivan V. Cockroft, Scott L. Cowley, Michael J. Reversible Reductive Elimination in Aluminum(II) Dihydrides |
title | Reversible Reductive Elimination in Aluminum(II) Dihydrides |
title_full | Reversible Reductive Elimination in Aluminum(II) Dihydrides |
title_fullStr | Reversible Reductive Elimination in Aluminum(II) Dihydrides |
title_full_unstemmed | Reversible Reductive Elimination in Aluminum(II) Dihydrides |
title_short | Reversible Reductive Elimination in Aluminum(II) Dihydrides |
title_sort | reversible reductive elimination in aluminum(ii) dihydrides |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7894477/ https://www.ncbi.nlm.nih.gov/pubmed/33022874 http://dx.doi.org/10.1002/anie.202011418 |
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