Efficient Synthesis of β-Enaminones and β-Enaminoesters Catalyzed by Gold (I)/Silver (I) under Solvent-Free Conditions

An efficient method for the synthesis of β-enaminones and β-enaminoesters using a combination of [(PPh(3))AuCl]/AgOTf as catalyst has been developed. The reaction between 1,3-dicarbonyl compounds and primary amines was carried out under solvent-free conditions with low catalyst loading in good to ex...

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Detalles Bibliográficos
Autores principales: Zhang, Ming, Abdukader, Ablimit, Fu, Yong, Zhu, Chengjian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
Materias:
Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268053/
https://www.ncbi.nlm.nih.gov/pubmed/22395409
http://dx.doi.org/10.3390/molecules17032812
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author Zhang, Ming
Abdukader, Ablimit
Fu, Yong
Zhu, Chengjian
author_facet Zhang, Ming
Abdukader, Ablimit
Fu, Yong
Zhu, Chengjian
author_sort Zhang, Ming
collection PubMed
description An efficient method for the synthesis of β-enaminones and β-enaminoesters using a combination of [(PPh(3))AuCl]/AgOTf as catalyst has been developed. The reaction between 1,3-dicarbonyl compounds and primary amines was carried out under solvent-free conditions with low catalyst loading in good to excellent yields at room temperature.
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spelling pubmed-62680532018-12-20 Efficient Synthesis of β-Enaminones and β-Enaminoesters Catalyzed by Gold (I)/Silver (I) under Solvent-Free Conditions Zhang, Ming Abdukader, Ablimit Fu, Yong Zhu, Chengjian Molecules Communication An efficient method for the synthesis of β-enaminones and β-enaminoesters using a combination of [(PPh(3))AuCl]/AgOTf as catalyst has been developed. The reaction between 1,3-dicarbonyl compounds and primary amines was carried out under solvent-free conditions with low catalyst loading in good to excellent yields at room temperature. MDPI 2012-03-06 /pmc/articles/PMC6268053/ /pubmed/22395409 http://dx.doi.org/10.3390/molecules17032812 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ 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 Communication
Zhang, Ming
Abdukader, Ablimit
Fu, Yong
Zhu, Chengjian
Efficient Synthesis of β-Enaminones and β-Enaminoesters Catalyzed by Gold (I)/Silver (I) under Solvent-Free Conditions
title Efficient Synthesis of β-Enaminones and β-Enaminoesters Catalyzed by Gold (I)/Silver (I) under Solvent-Free Conditions
title_full Efficient Synthesis of β-Enaminones and β-Enaminoesters Catalyzed by Gold (I)/Silver (I) under Solvent-Free Conditions
title_fullStr Efficient Synthesis of β-Enaminones and β-Enaminoesters Catalyzed by Gold (I)/Silver (I) under Solvent-Free Conditions
title_full_unstemmed Efficient Synthesis of β-Enaminones and β-Enaminoesters Catalyzed by Gold (I)/Silver (I) under Solvent-Free Conditions
title_short Efficient Synthesis of β-Enaminones and β-Enaminoesters Catalyzed by Gold (I)/Silver (I) under Solvent-Free Conditions
title_sort efficient synthesis of β-enaminones and β-enaminoesters catalyzed by gold (i)/silver (i) under solvent-free conditions
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268053/
https://www.ncbi.nlm.nih.gov/pubmed/22395409
http://dx.doi.org/10.3390/molecules17032812
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AT abdukaderablimit efficientsynthesisofbenaminonesandbenaminoesterscatalyzedbygoldisilveriundersolventfreeconditions
AT fuyong efficientsynthesisofbenaminonesandbenaminoesterscatalyzedbygoldisilveriundersolventfreeconditions
AT zhuchengjian efficientsynthesisofbenaminonesandbenaminoesterscatalyzedbygoldisilveriundersolventfreeconditions

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