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A Simple Iron-Catalyst for Alkenylation of Ketones Using Primary Alcohols

Herein, we developed a simple iron-catalyzed system for the α-alkenylation of ketones using primary alcohols. Such acceptor-less dehydrogenative coupling (ADC) of alcohols resulted in the synthesis of a series of important α,β-unsaturated functionalized ketones, having aryl, heteroaryl, alkyl, nitro...

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Detalles Bibliográficos
Autores principales: Sk, Motahar, Kumar, Ashish, Das, Jagadish, Banerjee, Debasis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7181299/
https://www.ncbi.nlm.nih.gov/pubmed/32235642
http://dx.doi.org/10.3390/molecules25071590
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author Sk, Motahar
Kumar, Ashish
Das, Jagadish
Banerjee, Debasis
author_facet Sk, Motahar
Kumar, Ashish
Das, Jagadish
Banerjee, Debasis
author_sort Sk, Motahar
collection PubMed
description Herein, we developed a simple iron-catalyzed system for the α-alkenylation of ketones using primary alcohols. Such acceptor-less dehydrogenative coupling (ADC) of alcohols resulted in the synthesis of a series of important α,β-unsaturated functionalized ketones, having aryl, heteroaryl, alkyl, nitro, nitrile and trifluoro-methyl, as well as halogen moieties, with excellent yields and selectivity. Initial mechanistic studies, including deuterium labeling experiments, determination of rate and order of the reaction, and quantitative determination of H(2) gas, were performed. The overall transformations produce water and dihydrogen as byproducts.
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spelling pubmed-71812992020-04-28 A Simple Iron-Catalyst for Alkenylation of Ketones Using Primary Alcohols Sk, Motahar Kumar, Ashish Das, Jagadish Banerjee, Debasis Molecules Article Herein, we developed a simple iron-catalyzed system for the α-alkenylation of ketones using primary alcohols. Such acceptor-less dehydrogenative coupling (ADC) of alcohols resulted in the synthesis of a series of important α,β-unsaturated functionalized ketones, having aryl, heteroaryl, alkyl, nitro, nitrile and trifluoro-methyl, as well as halogen moieties, with excellent yields and selectivity. Initial mechanistic studies, including deuterium labeling experiments, determination of rate and order of the reaction, and quantitative determination of H(2) gas, were performed. The overall transformations produce water and dihydrogen as byproducts. MDPI 2020-03-30 /pmc/articles/PMC7181299/ /pubmed/32235642 http://dx.doi.org/10.3390/molecules25071590 Text en © 2020 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
Sk, Motahar
Kumar, Ashish
Das, Jagadish
Banerjee, Debasis
A Simple Iron-Catalyst for Alkenylation of Ketones Using Primary Alcohols
title A Simple Iron-Catalyst for Alkenylation of Ketones Using Primary Alcohols
title_full A Simple Iron-Catalyst for Alkenylation of Ketones Using Primary Alcohols
title_fullStr A Simple Iron-Catalyst for Alkenylation of Ketones Using Primary Alcohols
title_full_unstemmed A Simple Iron-Catalyst for Alkenylation of Ketones Using Primary Alcohols
title_short A Simple Iron-Catalyst for Alkenylation of Ketones Using Primary Alcohols
title_sort simple iron-catalyst for alkenylation of ketones using primary alcohols
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7181299/
https://www.ncbi.nlm.nih.gov/pubmed/32235642
http://dx.doi.org/10.3390/molecules25071590
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