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Heterogeneously Catalyzed Pechmann Condensation Employing the Tailored Zn(0.925)Ti(0.075)O NPs: Synthesis of Coumarin

[Image: see text] A novel heterogeneous catalytic method was developed for the synthesis of coumarin and its derivatives using the Ti(IV)-doped ZnO matrix forming catalyst Zn(0.925)Ti(0.075)O having a high surface area and good Lewis acidity. The catalyst shows high activity toward a broad spectrum...

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Autores principales: Jadhav, Nirajkumar H., Sakate, Sachin S., Rasal, Nishant K., Shinde, Dnyaneshwar R., Pawar, Ramdas A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648791/
https://www.ncbi.nlm.nih.gov/pubmed/31459942
http://dx.doi.org/10.1021/acsomega.9b00257
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author Jadhav, Nirajkumar H.
Sakate, Sachin S.
Rasal, Nishant K.
Shinde, Dnyaneshwar R.
Pawar, Ramdas A.
author_facet Jadhav, Nirajkumar H.
Sakate, Sachin S.
Rasal, Nishant K.
Shinde, Dnyaneshwar R.
Pawar, Ramdas A.
author_sort Jadhav, Nirajkumar H.
collection PubMed
description [Image: see text] A novel heterogeneous catalytic method was developed for the synthesis of coumarin and its derivatives using the Ti(IV)-doped ZnO matrix forming catalyst Zn(0.925)Ti(0.075)O having a high surface area and good Lewis acidity. The catalyst shows high activity toward a broad spectrum of the substituted phenols with β-ketoesters such as ethyl acetoacetate, ethyl butyryl acetate, ethyl benzoyl acetate, and so forth in good yields over short reaction times during the synthesis of coumarins. The methodology was further extended for the synthesis of ayapin molecules. The catalyst also shows recycle activity up to seven cycles with very good stability.
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spelling pubmed-66487912019-08-27 Heterogeneously Catalyzed Pechmann Condensation Employing the Tailored Zn(0.925)Ti(0.075)O NPs: Synthesis of Coumarin Jadhav, Nirajkumar H. Sakate, Sachin S. Rasal, Nishant K. Shinde, Dnyaneshwar R. Pawar, Ramdas A. ACS Omega [Image: see text] A novel heterogeneous catalytic method was developed for the synthesis of coumarin and its derivatives using the Ti(IV)-doped ZnO matrix forming catalyst Zn(0.925)Ti(0.075)O having a high surface area and good Lewis acidity. The catalyst shows high activity toward a broad spectrum of the substituted phenols with β-ketoesters such as ethyl acetoacetate, ethyl butyryl acetate, ethyl benzoyl acetate, and so forth in good yields over short reaction times during the synthesis of coumarins. The methodology was further extended for the synthesis of ayapin molecules. The catalyst also shows recycle activity up to seven cycles with very good stability. American Chemical Society 2019-05-15 /pmc/articles/PMC6648791/ /pubmed/31459942 http://dx.doi.org/10.1021/acsomega.9b00257 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Jadhav, Nirajkumar H.
Sakate, Sachin S.
Rasal, Nishant K.
Shinde, Dnyaneshwar R.
Pawar, Ramdas A.
Heterogeneously Catalyzed Pechmann Condensation Employing the Tailored Zn(0.925)Ti(0.075)O NPs: Synthesis of Coumarin
title Heterogeneously Catalyzed Pechmann Condensation Employing the Tailored Zn(0.925)Ti(0.075)O NPs: Synthesis of Coumarin
title_full Heterogeneously Catalyzed Pechmann Condensation Employing the Tailored Zn(0.925)Ti(0.075)O NPs: Synthesis of Coumarin
title_fullStr Heterogeneously Catalyzed Pechmann Condensation Employing the Tailored Zn(0.925)Ti(0.075)O NPs: Synthesis of Coumarin
title_full_unstemmed Heterogeneously Catalyzed Pechmann Condensation Employing the Tailored Zn(0.925)Ti(0.075)O NPs: Synthesis of Coumarin
title_short Heterogeneously Catalyzed Pechmann Condensation Employing the Tailored Zn(0.925)Ti(0.075)O NPs: Synthesis of Coumarin
title_sort heterogeneously catalyzed pechmann condensation employing the tailored zn(0.925)ti(0.075)o nps: synthesis of coumarin
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648791/
https://www.ncbi.nlm.nih.gov/pubmed/31459942
http://dx.doi.org/10.1021/acsomega.9b00257
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