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Ag(2)O on ZrO(2) as a Recyclable Catalyst for Multicomponent Synthesis of Indenopyrimidine Derivatives

We describe the synthesis of silver loaded on zirconia and its use as an efficient catalyst for a one-pot three-component reaction to synthesize 11 indenopyrimidine derivatives, of which 7 are new compounds. The procedure involves substituted benzaldehydes, indane-1,3-dione, and guanidinium hydrochl...

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Autores principales: Bhaskaruni, Sandeep V. H. S., Maddila, Suresh, van Zyl, Werner E., Jonnalagadda, Sreekantha B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100188/
https://www.ncbi.nlm.nih.gov/pubmed/29976914
http://dx.doi.org/10.3390/molecules23071648
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author Bhaskaruni, Sandeep V. H. S.
Maddila, Suresh
van Zyl, Werner E.
Jonnalagadda, Sreekantha B.
author_facet Bhaskaruni, Sandeep V. H. S.
Maddila, Suresh
van Zyl, Werner E.
Jonnalagadda, Sreekantha B.
author_sort Bhaskaruni, Sandeep V. H. S.
collection PubMed
description We describe the synthesis of silver loaded on zirconia and its use as an efficient catalyst for a one-pot three-component reaction to synthesize 11 indenopyrimidine derivatives, of which 7 are new compounds. The procedure involves substituted benzaldehydes, indane-1,3-dione, and guanidinium hydrochloride, with ethanol as solvent. The proposed green protocol at room temperature is simple and efficient, giving excellent yields (90–96%) in short reaction times (<30 min). The protocol works well according to the green chemistry principles with respect to high atom economy, no need for column separation, and reusability of the catalyst, which are attractive features. XRD, TEM, SEM, and BET analysis were used to characterize the catalyst materials.
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spelling pubmed-61001882018-11-13 Ag(2)O on ZrO(2) as a Recyclable Catalyst for Multicomponent Synthesis of Indenopyrimidine Derivatives Bhaskaruni, Sandeep V. H. S. Maddila, Suresh van Zyl, Werner E. Jonnalagadda, Sreekantha B. Molecules Article We describe the synthesis of silver loaded on zirconia and its use as an efficient catalyst for a one-pot three-component reaction to synthesize 11 indenopyrimidine derivatives, of which 7 are new compounds. The procedure involves substituted benzaldehydes, indane-1,3-dione, and guanidinium hydrochloride, with ethanol as solvent. The proposed green protocol at room temperature is simple and efficient, giving excellent yields (90–96%) in short reaction times (<30 min). The protocol works well according to the green chemistry principles with respect to high atom economy, no need for column separation, and reusability of the catalyst, which are attractive features. XRD, TEM, SEM, and BET analysis were used to characterize the catalyst materials. MDPI 2018-07-05 /pmc/articles/PMC6100188/ /pubmed/29976914 http://dx.doi.org/10.3390/molecules23071648 Text en © 2018 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
Bhaskaruni, Sandeep V. H. S.
Maddila, Suresh
van Zyl, Werner E.
Jonnalagadda, Sreekantha B.
Ag(2)O on ZrO(2) as a Recyclable Catalyst for Multicomponent Synthesis of Indenopyrimidine Derivatives
title Ag(2)O on ZrO(2) as a Recyclable Catalyst for Multicomponent Synthesis of Indenopyrimidine Derivatives
title_full Ag(2)O on ZrO(2) as a Recyclable Catalyst for Multicomponent Synthesis of Indenopyrimidine Derivatives
title_fullStr Ag(2)O on ZrO(2) as a Recyclable Catalyst for Multicomponent Synthesis of Indenopyrimidine Derivatives
title_full_unstemmed Ag(2)O on ZrO(2) as a Recyclable Catalyst for Multicomponent Synthesis of Indenopyrimidine Derivatives
title_short Ag(2)O on ZrO(2) as a Recyclable Catalyst for Multicomponent Synthesis of Indenopyrimidine Derivatives
title_sort ag(2)o on zro(2) as a recyclable catalyst for multicomponent synthesis of indenopyrimidine derivatives
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100188/
https://www.ncbi.nlm.nih.gov/pubmed/29976914
http://dx.doi.org/10.3390/molecules23071648
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