Iron-containing mesoporous aluminosilicate catalyzed direct alkenylation of phenols: Facile synthesis of 1,1-diarylalkenes

The addition of phenols to aryl-substituted alkynes to form 1,1-diarylalkenes was carried out by using the Fe-Al-MCM-41 catalyst. The catalyst showed remarkable improvement in time and yield in comparison to other solid catalysts. The heterogeneous catalyst can be reused at least three times without...

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Detalles Bibliográficos
Autores principales: Haldar, Satyajit, Koner, Subratanath
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2013
Materias:
Full Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3566757/
https://www.ncbi.nlm.nih.gov/pubmed/23400112
http://dx.doi.org/10.3762/bjoc.9.6
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author Haldar, Satyajit
Koner, Subratanath
author_facet Haldar, Satyajit
Koner, Subratanath
author_sort Haldar, Satyajit
collection PubMed
description The addition of phenols to aryl-substituted alkynes to form 1,1-diarylalkenes was carried out by using the Fe-Al-MCM-41 catalyst. The catalyst showed remarkable improvement in time and yield in comparison to other solid catalysts. The heterogeneous catalyst can be reused at least three times without a significant loss in activity.
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spelling pubmed-35667572013-02-11 Iron-containing mesoporous aluminosilicate catalyzed direct alkenylation of phenols: Facile synthesis of 1,1-diarylalkenes Haldar, Satyajit Koner, Subratanath Beilstein J Org Chem Full Research Paper The addition of phenols to aryl-substituted alkynes to form 1,1-diarylalkenes was carried out by using the Fe-Al-MCM-41 catalyst. The catalyst showed remarkable improvement in time and yield in comparison to other solid catalysts. The heterogeneous catalyst can be reused at least three times without a significant loss in activity. Beilstein-Institut 2013-01-09 /pmc/articles/PMC3566757/ /pubmed/23400112 http://dx.doi.org/10.3762/bjoc.9.6 Text en Copyright © 2013, Haldar and Koner https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Haldar, Satyajit
Koner, Subratanath
Iron-containing mesoporous aluminosilicate catalyzed direct alkenylation of phenols: Facile synthesis of 1,1-diarylalkenes
title Iron-containing mesoporous aluminosilicate catalyzed direct alkenylation of phenols: Facile synthesis of 1,1-diarylalkenes
title_full Iron-containing mesoporous aluminosilicate catalyzed direct alkenylation of phenols: Facile synthesis of 1,1-diarylalkenes
title_fullStr Iron-containing mesoporous aluminosilicate catalyzed direct alkenylation of phenols: Facile synthesis of 1,1-diarylalkenes
title_full_unstemmed Iron-containing mesoporous aluminosilicate catalyzed direct alkenylation of phenols: Facile synthesis of 1,1-diarylalkenes
title_short Iron-containing mesoporous aluminosilicate catalyzed direct alkenylation of phenols: Facile synthesis of 1,1-diarylalkenes
title_sort iron-containing mesoporous aluminosilicate catalyzed direct alkenylation of phenols: facile synthesis of 1,1-diarylalkenes
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3566757/
https://www.ncbi.nlm.nih.gov/pubmed/23400112
http://dx.doi.org/10.3762/bjoc.9.6
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AT konersubratanath ironcontainingmesoporousaluminosilicatecatalyzeddirectalkenylationofphenolsfacilesynthesisof11diarylalkenes

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