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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...

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Autores principales: Martínez-Castro, Elisa, Suárez-Pantiga, Samuel, Mendoza, Abraham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
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.
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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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