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A tutorial review of stereoretentive olefin metathesis based on ruthenium dithiolate catalysts
Stereoretentive olefin metathesis based on ruthenium dithiolate complexes has become a very active field of research within the past years. This unique catalyst class is able to kinetically produce both Z- and E-alkenes in high stereochemical purity (typically >95:5) starting from stereochemicall...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Beilstein-Institut
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6296435/ https://www.ncbi.nlm.nih.gov/pubmed/30591823 http://dx.doi.org/10.3762/bjoc.14.279 |
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author | Müller, Daniel S Baslé, Olivier Mauduit, Marc |
author_facet | Müller, Daniel S Baslé, Olivier Mauduit, Marc |
author_sort | Müller, Daniel S |
collection | PubMed |
description | Stereoretentive olefin metathesis based on ruthenium dithiolate complexes has become a very active field of research within the past years. This unique catalyst class is able to kinetically produce both Z- and E-alkenes in high stereochemical purity (typically >95:5) starting from stereochemically pure Z- or E-alkenes. The aim of this tutorial review is to organize the reported information concerning ruthenium dithiolate catalysts in a logic manner, thus providing an "operators handbook" for chemists who wish to apply this methodology in synthesis. |
format | Online Article Text |
id | pubmed-6296435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-62964352018-12-27 A tutorial review of stereoretentive olefin metathesis based on ruthenium dithiolate catalysts Müller, Daniel S Baslé, Olivier Mauduit, Marc Beilstein J Org Chem Review Stereoretentive olefin metathesis based on ruthenium dithiolate complexes has become a very active field of research within the past years. This unique catalyst class is able to kinetically produce both Z- and E-alkenes in high stereochemical purity (typically >95:5) starting from stereochemically pure Z- or E-alkenes. The aim of this tutorial review is to organize the reported information concerning ruthenium dithiolate catalysts in a logic manner, thus providing an "operators handbook" for chemists who wish to apply this methodology in synthesis. Beilstein-Institut 2018-12-07 /pmc/articles/PMC6296435/ /pubmed/30591823 http://dx.doi.org/10.3762/bjoc.14.279 Text en Copyright © 2018, Müller et al. https://creativecommons.org/licenses/by/4.0https://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/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Review Müller, Daniel S Baslé, Olivier Mauduit, Marc A tutorial review of stereoretentive olefin metathesis based on ruthenium dithiolate catalysts |
title | A tutorial review of stereoretentive olefin metathesis based on ruthenium dithiolate catalysts |
title_full | A tutorial review of stereoretentive olefin metathesis based on ruthenium dithiolate catalysts |
title_fullStr | A tutorial review of stereoretentive olefin metathesis based on ruthenium dithiolate catalysts |
title_full_unstemmed | A tutorial review of stereoretentive olefin metathesis based on ruthenium dithiolate catalysts |
title_short | A tutorial review of stereoretentive olefin metathesis based on ruthenium dithiolate catalysts |
title_sort | tutorial review of stereoretentive olefin metathesis based on ruthenium dithiolate catalysts |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6296435/ https://www.ncbi.nlm.nih.gov/pubmed/30591823 http://dx.doi.org/10.3762/bjoc.14.279 |
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