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Beyond catalyst deactivation: cross-metathesis involving olefins containing N-heteroaromatics

Alkenes containing N-heteroaromatics are known to be poor partners in cross-metathesis reactions, probably due to catalyst deactivation caused by the presence of a nitrogen atom. However, some examples of ring-closing and cross-metathesis involving alkenes that incorporate N-heteroaromatics can be f...

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Detalles Bibliográficos
Autores principales: Lafaye, Kevin, Bosset, Cyril, Nicolas, Lionel, Guérinot, Amandine, Cossy, Janine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4660986/
https://www.ncbi.nlm.nih.gov/pubmed/26664645
http://dx.doi.org/10.3762/bjoc.11.241
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author Lafaye, Kevin
Bosset, Cyril
Nicolas, Lionel
Guérinot, Amandine
Cossy, Janine
author_facet Lafaye, Kevin
Bosset, Cyril
Nicolas, Lionel
Guérinot, Amandine
Cossy, Janine
author_sort Lafaye, Kevin
collection PubMed
description Alkenes containing N-heteroaromatics are known to be poor partners in cross-metathesis reactions, probably due to catalyst deactivation caused by the presence of a nitrogen atom. However, some examples of ring-closing and cross-metathesis involving alkenes that incorporate N-heteroaromatics can be found in the literature. In addition, recent mechanistic studies have focused on the rationalization of nitrogen-induced catalysts deactivation. The purpose of this mini-review is to give a brief overview of successful metathesis reactions involving olefins containing N-heteroaromatics in order to delineate some guidelines for the use of these challenging substrates in metathesis reactions.
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spelling pubmed-46609862015-12-09 Beyond catalyst deactivation: cross-metathesis involving olefins containing N-heteroaromatics Lafaye, Kevin Bosset, Cyril Nicolas, Lionel Guérinot, Amandine Cossy, Janine Beilstein J Org Chem Review Alkenes containing N-heteroaromatics are known to be poor partners in cross-metathesis reactions, probably due to catalyst deactivation caused by the presence of a nitrogen atom. However, some examples of ring-closing and cross-metathesis involving alkenes that incorporate N-heteroaromatics can be found in the literature. In addition, recent mechanistic studies have focused on the rationalization of nitrogen-induced catalysts deactivation. The purpose of this mini-review is to give a brief overview of successful metathesis reactions involving olefins containing N-heteroaromatics in order to delineate some guidelines for the use of these challenging substrates in metathesis reactions. Beilstein-Institut 2015-11-18 /pmc/articles/PMC4660986/ /pubmed/26664645 http://dx.doi.org/10.3762/bjoc.11.241 Text en Copyright © 2015, Lafaye 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 Review
Lafaye, Kevin
Bosset, Cyril
Nicolas, Lionel
Guérinot, Amandine
Cossy, Janine
Beyond catalyst deactivation: cross-metathesis involving olefins containing N-heteroaromatics
title Beyond catalyst deactivation: cross-metathesis involving olefins containing N-heteroaromatics
title_full Beyond catalyst deactivation: cross-metathesis involving olefins containing N-heteroaromatics
title_fullStr Beyond catalyst deactivation: cross-metathesis involving olefins containing N-heteroaromatics
title_full_unstemmed Beyond catalyst deactivation: cross-metathesis involving olefins containing N-heteroaromatics
title_short Beyond catalyst deactivation: cross-metathesis involving olefins containing N-heteroaromatics
title_sort beyond catalyst deactivation: cross-metathesis involving olefins containing n-heteroaromatics
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4660986/
https://www.ncbi.nlm.nih.gov/pubmed/26664645
http://dx.doi.org/10.3762/bjoc.11.241
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