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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(...

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Autores principales: Pham, Phuong T., Nguyen, Duyen K., Phan, Nam T. S., Le, Minh-Vien, Nguyen, Tung T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
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.
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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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