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Site-selective nitrenoid insertions utilizing postfunctionalized bifunctional rhodium(ii) catalysts

We report a new strategy for the preparation of dirhodium(ii) complexes with the general formula Rh(2)(A)(4) that allows the isolation of a dirhodium tetracarboxylate complex with a free amino group available for postfunctionalization. The postfunctionalization of this complex enables the incorporat...

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Autores principales: Berndt, Jan-Philipp, Radchenko, Yevhenii, Becker, Jonathan, Logemann, Christian, Bhandari, Dhaka R., Hrdina, Radim, Schreiner, Peter R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429793/
https://www.ncbi.nlm.nih.gov/pubmed/30996919
http://dx.doi.org/10.1039/c8sc05733h
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author Berndt, Jan-Philipp
Radchenko, Yevhenii
Becker, Jonathan
Logemann, Christian
Bhandari, Dhaka R.
Hrdina, Radim
Schreiner, Peter R.
author_facet Berndt, Jan-Philipp
Radchenko, Yevhenii
Becker, Jonathan
Logemann, Christian
Bhandari, Dhaka R.
Hrdina, Radim
Schreiner, Peter R.
author_sort Berndt, Jan-Philipp
collection PubMed
description We report a new strategy for the preparation of dirhodium(ii) complexes with the general formula Rh(2)(A)(4) that allows the isolation of a dirhodium tetracarboxylate complex with a free amino group available for postfunctionalization. The postfunctionalization of this complex enables the incorporation of a variety of functional groups, including double and triple bonds as well as nucleophilic moieties, thus paving the way to new classes of polymeric as well as bifunctional catalysts, and polymetallic complexes. Furthermore, we demonstrate that a urea containing dirhodium(ii) complex enables site-selective nitrenoid insertions by remote hydrogen bonding control.
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spelling pubmed-64297932019-04-17 Site-selective nitrenoid insertions utilizing postfunctionalized bifunctional rhodium(ii) catalysts Berndt, Jan-Philipp Radchenko, Yevhenii Becker, Jonathan Logemann, Christian Bhandari, Dhaka R. Hrdina, Radim Schreiner, Peter R. Chem Sci Chemistry We report a new strategy for the preparation of dirhodium(ii) complexes with the general formula Rh(2)(A)(4) that allows the isolation of a dirhodium tetracarboxylate complex with a free amino group available for postfunctionalization. The postfunctionalization of this complex enables the incorporation of a variety of functional groups, including double and triple bonds as well as nucleophilic moieties, thus paving the way to new classes of polymeric as well as bifunctional catalysts, and polymetallic complexes. Furthermore, we demonstrate that a urea containing dirhodium(ii) complex enables site-selective nitrenoid insertions by remote hydrogen bonding control. Royal Society of Chemistry 2019-02-06 /pmc/articles/PMC6429793/ /pubmed/30996919 http://dx.doi.org/10.1039/c8sc05733h Text en This journal is © The Royal Society of Chemistry 2019 https://creativecommons.org/licenses/by-nc/3.0/This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0)
spellingShingle Chemistry
Berndt, Jan-Philipp
Radchenko, Yevhenii
Becker, Jonathan
Logemann, Christian
Bhandari, Dhaka R.
Hrdina, Radim
Schreiner, Peter R.
Site-selective nitrenoid insertions utilizing postfunctionalized bifunctional rhodium(ii) catalysts
title Site-selective nitrenoid insertions utilizing postfunctionalized bifunctional rhodium(ii) catalysts
title_full Site-selective nitrenoid insertions utilizing postfunctionalized bifunctional rhodium(ii) catalysts
title_fullStr Site-selective nitrenoid insertions utilizing postfunctionalized bifunctional rhodium(ii) catalysts
title_full_unstemmed Site-selective nitrenoid insertions utilizing postfunctionalized bifunctional rhodium(ii) catalysts
title_short Site-selective nitrenoid insertions utilizing postfunctionalized bifunctional rhodium(ii) catalysts
title_sort site-selective nitrenoid insertions utilizing postfunctionalized bifunctional rhodium(ii) catalysts
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429793/
https://www.ncbi.nlm.nih.gov/pubmed/30996919
http://dx.doi.org/10.1039/c8sc05733h
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