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New metathesis catalyst bearing chromanyl moieties at the N-heterocyclic carbene ligand
The synthesis of a new type of Hoveyda–Grubbs 2(nd) generation catalyst bearing a modified N-heterocyclic carbene ligands is reported. The new catalyst contains an NHC ligand symmetrically substituted with chromanyl moieties. The complex was tested in model CM and RCM reactions. It showed very high...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4734414/ https://www.ncbi.nlm.nih.gov/pubmed/26877801 http://dx.doi.org/10.3762/bjoc.11.300 |
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author | Hryniewicka, Agnieszka Suchodolski, Szymon Wojtkielewicz, Agnieszka Morzycki, Jacek W Witkowski, Stanisław |
author_facet | Hryniewicka, Agnieszka Suchodolski, Szymon Wojtkielewicz, Agnieszka Morzycki, Jacek W Witkowski, Stanisław |
author_sort | Hryniewicka, Agnieszka |
collection | PubMed |
description | The synthesis of a new type of Hoveyda–Grubbs 2(nd) generation catalyst bearing a modified N-heterocyclic carbene ligands is reported. The new catalyst contains an NHC ligand symmetrically substituted with chromanyl moieties. The complex was tested in model CM and RCM reactions. It showed very high activity in CM reactions with electron-deficient α,β-unsaturated compounds even at 0 °C. It was also examined in more demanding systems such as conjugated dienes and polyenes. The catalyst is stable, storable and easy to purify. |
format | Online Article Text |
id | pubmed-4734414 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-47344142016-02-12 New metathesis catalyst bearing chromanyl moieties at the N-heterocyclic carbene ligand Hryniewicka, Agnieszka Suchodolski, Szymon Wojtkielewicz, Agnieszka Morzycki, Jacek W Witkowski, Stanisław Beilstein J Org Chem Full Research Paper The synthesis of a new type of Hoveyda–Grubbs 2(nd) generation catalyst bearing a modified N-heterocyclic carbene ligands is reported. The new catalyst contains an NHC ligand symmetrically substituted with chromanyl moieties. The complex was tested in model CM and RCM reactions. It showed very high activity in CM reactions with electron-deficient α,β-unsaturated compounds even at 0 °C. It was also examined in more demanding systems such as conjugated dienes and polyenes. The catalyst is stable, storable and easy to purify. Beilstein-Institut 2015-12-30 /pmc/articles/PMC4734414/ /pubmed/26877801 http://dx.doi.org/10.3762/bjoc.11.300 Text en Copyright © 2015, Hryniewicka et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Hryniewicka, Agnieszka Suchodolski, Szymon Wojtkielewicz, Agnieszka Morzycki, Jacek W Witkowski, Stanisław New metathesis catalyst bearing chromanyl moieties at the N-heterocyclic carbene ligand |
title | New metathesis catalyst bearing chromanyl moieties at the N-heterocyclic carbene ligand |
title_full | New metathesis catalyst bearing chromanyl moieties at the N-heterocyclic carbene ligand |
title_fullStr | New metathesis catalyst bearing chromanyl moieties at the N-heterocyclic carbene ligand |
title_full_unstemmed | New metathesis catalyst bearing chromanyl moieties at the N-heterocyclic carbene ligand |
title_short | New metathesis catalyst bearing chromanyl moieties at the N-heterocyclic carbene ligand |
title_sort | new metathesis catalyst bearing chromanyl moieties at the n-heterocyclic carbene ligand |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4734414/ https://www.ncbi.nlm.nih.gov/pubmed/26877801 http://dx.doi.org/10.3762/bjoc.11.300 |
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