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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...

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Detalles Bibliográficos
Autores principales: Müller, Daniel S, Baslé, Olivier, Mauduit, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2018
Materias:
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.
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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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