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Oxidative annulation of acetophenones and 2-aminobenzothiazoles catalyzed by reusable nickel-doped LaMnO(3) perovskites
Synthesis of imidazole[2,1-b]benzothiazoles often suffers from the use of pre-functionalized substrates and/or homogeneous, non-recyclable catalytic systems. Herein we report a method for direct coupling of acetophenones and 2-aminobenzothiazoles in the presence of reusable perovskites, namely LaMn(...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9869463/ https://www.ncbi.nlm.nih.gov/pubmed/36756421 http://dx.doi.org/10.1039/d2ra08045a |
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author | Pham, Phuong T. Nguyen, Duyen K. Phan, Nam T. S. Le, Minh-Vien Nguyen, Tung T. |
author_facet | Pham, Phuong T. Nguyen, Duyen K. Phan, Nam T. S. Le, Minh-Vien Nguyen, Tung T. |
author_sort | Pham, Phuong T. |
collection | PubMed |
description | Synthesis of imidazole[2,1-b]benzothiazoles often suffers from the use of pre-functionalized substrates and/or homogeneous, non-recyclable catalytic systems. Herein we report a method for direct coupling of acetophenones and 2-aminobenzothiazoles in the presence of reusable perovskites, namely LaMn(0.95)Ni(0.05)O(3). Imidazole[2,1-b]benzothiazoles were obtained in moderate to good yields and contained an array of useful functionalities. Control experiments indicated that the perovskites played pivotal roles in halogenation and condensation steps. |
format | Online Article Text |
id | pubmed-9869463 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-98694632023-02-07 Oxidative annulation of acetophenones and 2-aminobenzothiazoles catalyzed by reusable nickel-doped LaMnO(3) perovskites Pham, Phuong T. Nguyen, Duyen K. Phan, Nam T. S. Le, Minh-Vien Nguyen, Tung T. RSC Adv Chemistry Synthesis of imidazole[2,1-b]benzothiazoles often suffers from the use of pre-functionalized substrates and/or homogeneous, non-recyclable catalytic systems. Herein we report a method for direct coupling of acetophenones and 2-aminobenzothiazoles in the presence of reusable perovskites, namely LaMn(0.95)Ni(0.05)O(3). Imidazole[2,1-b]benzothiazoles were obtained in moderate to good yields and contained an array of useful functionalities. Control experiments indicated that the perovskites played pivotal roles in halogenation and condensation steps. The Royal Society of Chemistry 2023-01-23 /pmc/articles/PMC9869463/ /pubmed/36756421 http://dx.doi.org/10.1039/d2ra08045a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Pham, Phuong T. Nguyen, Duyen K. Phan, Nam T. S. Le, Minh-Vien Nguyen, Tung T. Oxidative annulation of acetophenones and 2-aminobenzothiazoles catalyzed by reusable nickel-doped LaMnO(3) perovskites |
title | Oxidative annulation of acetophenones and 2-aminobenzothiazoles catalyzed by reusable nickel-doped LaMnO(3) perovskites |
title_full | Oxidative annulation of acetophenones and 2-aminobenzothiazoles catalyzed by reusable nickel-doped LaMnO(3) perovskites |
title_fullStr | Oxidative annulation of acetophenones and 2-aminobenzothiazoles catalyzed by reusable nickel-doped LaMnO(3) perovskites |
title_full_unstemmed | Oxidative annulation of acetophenones and 2-aminobenzothiazoles catalyzed by reusable nickel-doped LaMnO(3) perovskites |
title_short | Oxidative annulation of acetophenones and 2-aminobenzothiazoles catalyzed by reusable nickel-doped LaMnO(3) perovskites |
title_sort | oxidative annulation of acetophenones and 2-aminobenzothiazoles catalyzed by reusable nickel-doped lamno(3) perovskites |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9869463/ https://www.ncbi.nlm.nih.gov/pubmed/36756421 http://dx.doi.org/10.1039/d2ra08045a |
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