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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...

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Autores principales: Hryniewicka, Agnieszka, Suchodolski, Szymon, Wojtkielewicz, Agnieszka, Morzycki, Jacek W, Witkowski, Stanisław
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2015
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.
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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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