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Synthesis of Known and Previously Inaccessible Poly(pyrazolyl)Borates under Mild Conditions

[Image: see text] Poly(pyrazolyl)borate ligands have been obtained through the reaction of highly reactive haloboranes with in situ formed pyrazolides under very mild conditions. This versatile synthetic method allows the selective synthesis of bis-, tris-, or tetrakis(pyrazolyl)borates. Furthermore...

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Autores principales: Melero, María M., Kłosek, Zuzanna, Ramírez de Arellano, Carmen, Olmos, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10337037/
https://www.ncbi.nlm.nih.gov/pubmed/37345738
http://dx.doi.org/10.1021/acs.joc.3c00761
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author Melero, María M.
Kłosek, Zuzanna
Ramírez de Arellano, Carmen
Olmos, Andrea
author_facet Melero, María M.
Kłosek, Zuzanna
Ramírez de Arellano, Carmen
Olmos, Andrea
author_sort Melero, María M.
collection PubMed
description [Image: see text] Poly(pyrazolyl)borate ligands have been obtained through the reaction of highly reactive haloboranes with in situ formed pyrazolides under very mild conditions. This versatile synthetic method allows the selective synthesis of bis-, tris-, or tetrakis(pyrazolyl)borates. Furthermore, the method is compatible with the use of functional groups on the heterocyclic moieties of the poly(pyrazolyl)borates that were not accessible to date. Strongly encumbered sodium and thallium(I) poly(pyrazolyl)borates with a reduced donating ability have been obtained for the first time.
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spelling pubmed-103370372023-07-13 Synthesis of Known and Previously Inaccessible Poly(pyrazolyl)Borates under Mild Conditions Melero, María M. Kłosek, Zuzanna Ramírez de Arellano, Carmen Olmos, Andrea J Org Chem [Image: see text] Poly(pyrazolyl)borate ligands have been obtained through the reaction of highly reactive haloboranes with in situ formed pyrazolides under very mild conditions. This versatile synthetic method allows the selective synthesis of bis-, tris-, or tetrakis(pyrazolyl)borates. Furthermore, the method is compatible with the use of functional groups on the heterocyclic moieties of the poly(pyrazolyl)borates that were not accessible to date. Strongly encumbered sodium and thallium(I) poly(pyrazolyl)borates with a reduced donating ability have been obtained for the first time. American Chemical Society 2023-06-22 /pmc/articles/PMC10337037/ /pubmed/37345738 http://dx.doi.org/10.1021/acs.joc.3c00761 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Melero, María M.
Kłosek, Zuzanna
Ramírez de Arellano, Carmen
Olmos, Andrea
Synthesis of Known and Previously Inaccessible Poly(pyrazolyl)Borates under Mild Conditions
title Synthesis of Known and Previously Inaccessible Poly(pyrazolyl)Borates under Mild Conditions
title_full Synthesis of Known and Previously Inaccessible Poly(pyrazolyl)Borates under Mild Conditions
title_fullStr Synthesis of Known and Previously Inaccessible Poly(pyrazolyl)Borates under Mild Conditions
title_full_unstemmed Synthesis of Known and Previously Inaccessible Poly(pyrazolyl)Borates under Mild Conditions
title_short Synthesis of Known and Previously Inaccessible Poly(pyrazolyl)Borates under Mild Conditions
title_sort synthesis of known and previously inaccessible poly(pyrazolyl)borates under mild conditions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10337037/
https://www.ncbi.nlm.nih.gov/pubmed/37345738
http://dx.doi.org/10.1021/acs.joc.3c00761
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