Hydrogenation of aromatic ketones, aldehydes, and epoxides with hydrogen and Pd(0)EnCat™ 30NP

Aromatic aldehydes and ketones as well as aromatic epoxides are selectively reduced to the corresponding alcohols under mild conditions using conventional hydrogen in the presence of Pd(0)EnCat™ 30NP catalyst. The reactions were performed at room temperature during 16 hours with high to excellent co...

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Detalles Bibliográficos
Autores principales: Ley, Steven V, Stewart-Liddon, Angus J P, Pears, David, Perni, Remedios H, Treacher, Kevin
Formato: Texto
Lenguaje:English
Publicado: Beilstein-Institut 2006
Materias:
Full Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1630636/
https://www.ncbi.nlm.nih.gov/pubmed/16934142
http://dx.doi.org/10.1186/1860-5397-2-15
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author Ley, Steven V
Stewart-Liddon, Angus J P
Pears, David
Perni, Remedios H
Treacher, Kevin
author_facet Ley, Steven V
Stewart-Liddon, Angus J P
Pears, David
Perni, Remedios H
Treacher, Kevin
author_sort Ley, Steven V
collection PubMed
description Aromatic aldehydes and ketones as well as aromatic epoxides are selectively reduced to the corresponding alcohols under mild conditions using conventional hydrogen in the presence of Pd(0)EnCat™ 30NP catalyst. The reactions were performed at room temperature during 16 hours with high to excellent conversions of the corresponding products.
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spelling pubmed-16306362006-11-02 Hydrogenation of aromatic ketones, aldehydes, and epoxides with hydrogen and Pd(0)EnCat™ 30NP Ley, Steven V Stewart-Liddon, Angus J P Pears, David Perni, Remedios H Treacher, Kevin Beilstein J Org Chem Full Research Paper Aromatic aldehydes and ketones as well as aromatic epoxides are selectively reduced to the corresponding alcohols under mild conditions using conventional hydrogen in the presence of Pd(0)EnCat™ 30NP catalyst. The reactions were performed at room temperature during 16 hours with high to excellent conversions of the corresponding products. Beilstein-Institut 2006-08-25 /pmc/articles/PMC1630636/ /pubmed/16934142 http://dx.doi.org/10.1186/1860-5397-2-15 Text en Copyright © 2006, Ley 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
Ley, Steven V
Stewart-Liddon, Angus J P
Pears, David
Perni, Remedios H
Treacher, Kevin
Hydrogenation of aromatic ketones, aldehydes, and epoxides with hydrogen and Pd(0)EnCat™ 30NP
title Hydrogenation of aromatic ketones, aldehydes, and epoxides with hydrogen and Pd(0)EnCat™ 30NP
title_full Hydrogenation of aromatic ketones, aldehydes, and epoxides with hydrogen and Pd(0)EnCat™ 30NP
title_fullStr Hydrogenation of aromatic ketones, aldehydes, and epoxides with hydrogen and Pd(0)EnCat™ 30NP
title_full_unstemmed Hydrogenation of aromatic ketones, aldehydes, and epoxides with hydrogen and Pd(0)EnCat™ 30NP
title_short Hydrogenation of aromatic ketones, aldehydes, and epoxides with hydrogen and Pd(0)EnCat™ 30NP
title_sort hydrogenation of aromatic ketones, aldehydes, and epoxides with hydrogen and pd(0)encat™ 30np
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1630636/
https://www.ncbi.nlm.nih.gov/pubmed/16934142
http://dx.doi.org/10.1186/1860-5397-2-15
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