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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...

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Detalles Bibliográficos
Autores principales: Gu, Xin, Wang, Xiaoyan, Wang, Fengtian, Sun, Hongbao, Liu, Jie, Xie, Yongmei, Xiang, Mingli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
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.
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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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