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Scalable Synthesis of Esp and Rhodium(II) Carboxylates from Acetylacetone and RhCl(3)·xH(2)O
[Image: see text] Rhodium(II) carboxylates are privileged catalysts for the most challenging carbene-, nitrene-, and oxo-transfer reactions. In this work, we address the strategic challenges of current organic and inorganic synthesis methods to access these rhodium(II) complexes through an oxidative...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7309316/ https://www.ncbi.nlm.nih.gov/pubmed/32587455 http://dx.doi.org/10.1021/acs.oprd.0c00164 |
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author | Martínez-Castro, Elisa Suárez-Pantiga, Samuel Mendoza, Abraham |
author_facet | Martínez-Castro, Elisa Suárez-Pantiga, Samuel Mendoza, Abraham |
author_sort | Martínez-Castro, Elisa |
collection | PubMed |
description | [Image: see text] Rhodium(II) carboxylates are privileged catalysts for the most challenging carbene-, nitrene-, and oxo-transfer reactions. In this work, we address the strategic challenges of current organic and inorganic synthesis methods to access these rhodium(II) complexes through an oxidative rearrangement strategy and a reductive ligation reaction. These studies illustrate the multiple benefits of oxidative rearrangement in the process-scale synthesis of congested carboxylates over nitrile anion alkylation reactions, and the impressive effect of inorganic additives in the reductive ligation of rhodium(III) salts. |
format | Online Article Text |
id | pubmed-7309316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-73093162020-06-23 Scalable Synthesis of Esp and Rhodium(II) Carboxylates from Acetylacetone and RhCl(3)·xH(2)O Martínez-Castro, Elisa Suárez-Pantiga, Samuel Mendoza, Abraham Org Process Res Dev [Image: see text] Rhodium(II) carboxylates are privileged catalysts for the most challenging carbene-, nitrene-, and oxo-transfer reactions. In this work, we address the strategic challenges of current organic and inorganic synthesis methods to access these rhodium(II) complexes through an oxidative rearrangement strategy and a reductive ligation reaction. These studies illustrate the multiple benefits of oxidative rearrangement in the process-scale synthesis of congested carboxylates over nitrile anion alkylation reactions, and the impressive effect of inorganic additives in the reductive ligation of rhodium(III) salts. American Chemical Society 2020-04-14 2020-06-19 /pmc/articles/PMC7309316/ /pubmed/32587455 http://dx.doi.org/10.1021/acs.oprd.0c00164 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Martínez-Castro, Elisa Suárez-Pantiga, Samuel Mendoza, Abraham Scalable Synthesis of Esp and Rhodium(II) Carboxylates from Acetylacetone and RhCl(3)·xH(2)O |
title | Scalable Synthesis of Esp and Rhodium(II) Carboxylates
from Acetylacetone and RhCl(3)·xH(2)O |
title_full | Scalable Synthesis of Esp and Rhodium(II) Carboxylates
from Acetylacetone and RhCl(3)·xH(2)O |
title_fullStr | Scalable Synthesis of Esp and Rhodium(II) Carboxylates
from Acetylacetone and RhCl(3)·xH(2)O |
title_full_unstemmed | Scalable Synthesis of Esp and Rhodium(II) Carboxylates
from Acetylacetone and RhCl(3)·xH(2)O |
title_short | Scalable Synthesis of Esp and Rhodium(II) Carboxylates
from Acetylacetone and RhCl(3)·xH(2)O |
title_sort | scalable synthesis of esp and rhodium(ii) carboxylates
from acetylacetone and rhcl(3)·xh(2)o |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7309316/ https://www.ncbi.nlm.nih.gov/pubmed/32587455 http://dx.doi.org/10.1021/acs.oprd.0c00164 |
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