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Vancomycin-Iridium (III) Interaction: An Unexplored Route for Enantioselective Imine Reduction
The chiral structure of antibiotic vancomycin (Van) was exploited as an innovative coordination sphere for the preparation of an IrCp* based hybrid catalysts. We found that Van is able to coordinate iridium (Ir(III)) and the complexation was demonstrated by several analytical techniques such as MALD...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6695689/ https://www.ncbi.nlm.nih.gov/pubmed/31366120 http://dx.doi.org/10.3390/molecules24152771 |
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author | Facchetti, Giorgio Pellegrino, Sara Bucci, Raffaella Nava, Donatella Gandolfi, Raffaella Christodoulou, Michael S. Rimoldi, Isabella |
author_facet | Facchetti, Giorgio Pellegrino, Sara Bucci, Raffaella Nava, Donatella Gandolfi, Raffaella Christodoulou, Michael S. Rimoldi, Isabella |
author_sort | Facchetti, Giorgio |
collection | PubMed |
description | The chiral structure of antibiotic vancomycin (Van) was exploited as an innovative coordination sphere for the preparation of an IrCp* based hybrid catalysts. We found that Van is able to coordinate iridium (Ir(III)) and the complexation was demonstrated by several analytical techniques such as MALDI-TOF, UV, Circular dichroism (CD), Raman IR, and NMR. The hybrid system so obtained was employed in the Asymmetric Transfer Hydrogenation (ATH) of cyclic imines allowing to obtain a valuable 61% e.e. (R) in the asymmetric reduction of quinaldine 2. The catalytic system exhibited a saturation kinetics with a calculated efficiency of K(cat)/K(M) = 0.688 h(−1)mM(−1). |
format | Online Article Text |
id | pubmed-6695689 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66956892019-09-05 Vancomycin-Iridium (III) Interaction: An Unexplored Route for Enantioselective Imine Reduction Facchetti, Giorgio Pellegrino, Sara Bucci, Raffaella Nava, Donatella Gandolfi, Raffaella Christodoulou, Michael S. Rimoldi, Isabella Molecules Communication The chiral structure of antibiotic vancomycin (Van) was exploited as an innovative coordination sphere for the preparation of an IrCp* based hybrid catalysts. We found that Van is able to coordinate iridium (Ir(III)) and the complexation was demonstrated by several analytical techniques such as MALDI-TOF, UV, Circular dichroism (CD), Raman IR, and NMR. The hybrid system so obtained was employed in the Asymmetric Transfer Hydrogenation (ATH) of cyclic imines allowing to obtain a valuable 61% e.e. (R) in the asymmetric reduction of quinaldine 2. The catalytic system exhibited a saturation kinetics with a calculated efficiency of K(cat)/K(M) = 0.688 h(−1)mM(−1). MDPI 2019-07-30 /pmc/articles/PMC6695689/ /pubmed/31366120 http://dx.doi.org/10.3390/molecules24152771 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Facchetti, Giorgio Pellegrino, Sara Bucci, Raffaella Nava, Donatella Gandolfi, Raffaella Christodoulou, Michael S. Rimoldi, Isabella Vancomycin-Iridium (III) Interaction: An Unexplored Route for Enantioselective Imine Reduction |
title | Vancomycin-Iridium (III) Interaction: An Unexplored Route for Enantioselective Imine Reduction |
title_full | Vancomycin-Iridium (III) Interaction: An Unexplored Route for Enantioselective Imine Reduction |
title_fullStr | Vancomycin-Iridium (III) Interaction: An Unexplored Route for Enantioselective Imine Reduction |
title_full_unstemmed | Vancomycin-Iridium (III) Interaction: An Unexplored Route for Enantioselective Imine Reduction |
title_short | Vancomycin-Iridium (III) Interaction: An Unexplored Route for Enantioselective Imine Reduction |
title_sort | vancomycin-iridium (iii) interaction: an unexplored route for enantioselective imine reduction |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6695689/ https://www.ncbi.nlm.nih.gov/pubmed/31366120 http://dx.doi.org/10.3390/molecules24152771 |
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