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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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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. |
format | Online Article Text |
id | pubmed-7181299 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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