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Pyrrolidine-Mediated Direct Preparation of (E)-Monoarylidene Derivatives of Homo- and Heterocyclic Ketones with Various Aldehydes
An efficient method for the facile synthesis of (E)-monoarylidene derivatives of homo- and heterocyclic ketones with various aldehydes in the presence of a pyrrolidine organocatalyst has been achieved. A range of α,β-unsaturated ketones were obtained in moderate to high yields (up to 99%). Unlike th...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271378/ https://www.ncbi.nlm.nih.gov/pubmed/24526254 http://dx.doi.org/10.3390/molecules19021976 |
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author | Gu, Xin Wang, Xiaoyan Wang, Fengtian Sun, Hongbao Liu, Jie Xie, Yongmei Xiang, Mingli |
author_facet | Gu, Xin Wang, Xiaoyan Wang, Fengtian Sun, Hongbao Liu, Jie Xie, Yongmei Xiang, Mingli |
author_sort | Gu, Xin |
collection | PubMed |
description | An efficient method for the facile synthesis of (E)-monoarylidene derivatives of homo- and heterocyclic ketones with various aldehydes in the presence of a pyrrolidine organocatalyst has been achieved. A range of α,β-unsaturated ketones were obtained in moderate to high yields (up to 99%). Unlike the Claisen-Schmidt condensation process, the formation of undesired bisarylidene byproducts is not observed. The possible reaction mechanism suggests that the reaction proceeds via a Mannich-elimination sequence. |
format | Online Article Text |
id | pubmed-6271378 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62713782018-12-20 Pyrrolidine-Mediated Direct Preparation of (E)-Monoarylidene Derivatives of Homo- and Heterocyclic Ketones with Various Aldehydes Gu, Xin Wang, Xiaoyan Wang, Fengtian Sun, Hongbao Liu, Jie Xie, Yongmei Xiang, Mingli Molecules Article An efficient method for the facile synthesis of (E)-monoarylidene derivatives of homo- and heterocyclic ketones with various aldehydes in the presence of a pyrrolidine organocatalyst has been achieved. A range of α,β-unsaturated ketones were obtained in moderate to high yields (up to 99%). Unlike the Claisen-Schmidt condensation process, the formation of undesired bisarylidene byproducts is not observed. The possible reaction mechanism suggests that the reaction proceeds via a Mannich-elimination sequence. MDPI 2014-02-12 /pmc/articles/PMC6271378/ /pubmed/24526254 http://dx.doi.org/10.3390/molecules19021976 Text en © 2014 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 license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Gu, Xin Wang, Xiaoyan Wang, Fengtian Sun, Hongbao Liu, Jie Xie, Yongmei Xiang, Mingli Pyrrolidine-Mediated Direct Preparation of (E)-Monoarylidene Derivatives of Homo- and Heterocyclic Ketones with Various Aldehydes |
title | Pyrrolidine-Mediated Direct Preparation of (E)-Monoarylidene Derivatives of Homo- and Heterocyclic Ketones with Various Aldehydes |
title_full | Pyrrolidine-Mediated Direct Preparation of (E)-Monoarylidene Derivatives of Homo- and Heterocyclic Ketones with Various Aldehydes |
title_fullStr | Pyrrolidine-Mediated Direct Preparation of (E)-Monoarylidene Derivatives of Homo- and Heterocyclic Ketones with Various Aldehydes |
title_full_unstemmed | Pyrrolidine-Mediated Direct Preparation of (E)-Monoarylidene Derivatives of Homo- and Heterocyclic Ketones with Various Aldehydes |
title_short | Pyrrolidine-Mediated Direct Preparation of (E)-Monoarylidene Derivatives of Homo- and Heterocyclic Ketones with Various Aldehydes |
title_sort | pyrrolidine-mediated direct preparation of (e)-monoarylidene derivatives of homo- and heterocyclic ketones with various aldehydes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271378/ https://www.ncbi.nlm.nih.gov/pubmed/24526254 http://dx.doi.org/10.3390/molecules19021976 |
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