Enantiomerically Enriched 1,2-P,N-Bidentate Ferrocenyl Ligands for 1,3-Dipolar Cycloaddition and Transfer Hydrogenation Reactions

Novel complexes of 1,2-P,N-bidentate ferrocenyl ligands with AgOAc or with [RuCl(2)(PPh(3))(3)] as catalysts have been studied in asymmetric synthesis. The catalytic activity of these systems have been studied in [3+2]-cycloaddition of azomethine ylides with olefins and the asymmetric transfer hydro...

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Autores principales: Utepova, Irina A., Serebrennikova, Polina O., Streltsova, Marina S., Musikhina, Alexandra A., Fedorchenko, Tatiana G., Chupakhin, Oleg N., Antonchick, Andrey P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100496/
https://www.ncbi.nlm.nih.gov/pubmed/29848984
http://dx.doi.org/10.3390/molecules23061311
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author Utepova, Irina A.
Serebrennikova, Polina O.
Streltsova, Marina S.
Musikhina, Alexandra A.
Fedorchenko, Tatiana G.
Chupakhin, Oleg N.
Antonchick, Andrey P.
author_facet Utepova, Irina A.
Serebrennikova, Polina O.
Streltsova, Marina S.
Musikhina, Alexandra A.
Fedorchenko, Tatiana G.
Chupakhin, Oleg N.
Antonchick, Andrey P.
author_sort Utepova, Irina A.
collection PubMed
description Novel complexes of 1,2-P,N-bidentate ferrocenyl ligands with AgOAc or with [RuCl(2)(PPh(3))(3)] as catalysts have been studied in asymmetric synthesis. The catalytic activity of these systems have been studied in [3+2]-cycloaddition of azomethine ylides with olefins and the asymmetric transfer hydrogenation of ketones.
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spelling pubmed-61004962018-11-13 Enantiomerically Enriched 1,2-P,N-Bidentate Ferrocenyl Ligands for 1,3-Dipolar Cycloaddition and Transfer Hydrogenation Reactions Utepova, Irina A. Serebrennikova, Polina O. Streltsova, Marina S. Musikhina, Alexandra A. Fedorchenko, Tatiana G. Chupakhin, Oleg N. Antonchick, Andrey P. Molecules Article Novel complexes of 1,2-P,N-bidentate ferrocenyl ligands with AgOAc or with [RuCl(2)(PPh(3))(3)] as catalysts have been studied in asymmetric synthesis. The catalytic activity of these systems have been studied in [3+2]-cycloaddition of azomethine ylides with olefins and the asymmetric transfer hydrogenation of ketones. MDPI 2018-05-30 /pmc/articles/PMC6100496/ /pubmed/29848984 http://dx.doi.org/10.3390/molecules23061311 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Utepova, Irina A.
Serebrennikova, Polina O.
Streltsova, Marina S.
Musikhina, Alexandra A.
Fedorchenko, Tatiana G.
Chupakhin, Oleg N.
Antonchick, Andrey P.
Enantiomerically Enriched 1,2-P,N-Bidentate Ferrocenyl Ligands for 1,3-Dipolar Cycloaddition and Transfer Hydrogenation Reactions
title Enantiomerically Enriched 1,2-P,N-Bidentate Ferrocenyl Ligands for 1,3-Dipolar Cycloaddition and Transfer Hydrogenation Reactions
title_full Enantiomerically Enriched 1,2-P,N-Bidentate Ferrocenyl Ligands for 1,3-Dipolar Cycloaddition and Transfer Hydrogenation Reactions
title_fullStr Enantiomerically Enriched 1,2-P,N-Bidentate Ferrocenyl Ligands for 1,3-Dipolar Cycloaddition and Transfer Hydrogenation Reactions
title_full_unstemmed Enantiomerically Enriched 1,2-P,N-Bidentate Ferrocenyl Ligands for 1,3-Dipolar Cycloaddition and Transfer Hydrogenation Reactions
title_short Enantiomerically Enriched 1,2-P,N-Bidentate Ferrocenyl Ligands for 1,3-Dipolar Cycloaddition and Transfer Hydrogenation Reactions
title_sort enantiomerically enriched 1,2-p,n-bidentate ferrocenyl ligands for 1,3-dipolar cycloaddition and transfer hydrogenation reactions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100496/
https://www.ncbi.nlm.nih.gov/pubmed/29848984
http://dx.doi.org/10.3390/molecules23061311
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