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Microwave Assisted Synthesis, Antifungal Activity, and DFT Study of Some Novel Triazolinone Derivatives

A series of some novel 1,2,4-triazol-5(4H)-one derivatives were designed and synthesized under microwave irradiation via multistep reaction. The structures of 1,2,4-triazoles were confirmed by (1)H NMR, MS, FTIR, and elemental analysis. The antifungal activities of 1,2,4-triazoles were determined. T...

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Detalles Bibliográficos
Autores principales: Sun, Na-Bo, Jin, Jian-Zhong, He, Fang-Yue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377350/
https://www.ncbi.nlm.nih.gov/pubmed/25861651
http://dx.doi.org/10.1155/2015/916059
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author Sun, Na-Bo
Jin, Jian-Zhong
He, Fang-Yue
author_facet Sun, Na-Bo
Jin, Jian-Zhong
He, Fang-Yue
author_sort Sun, Na-Bo
collection PubMed
description A series of some novel 1,2,4-triazol-5(4H)-one derivatives were designed and synthesized under microwave irradiation via multistep reaction. The structures of 1,2,4-triazoles were confirmed by (1)H NMR, MS, FTIR, and elemental analysis. The antifungal activities of 1,2,4-triazoles were determined. The antifungal activity results indicated that the compounds 5c, 5f, and 5h exhibited good activity against Pythium ultimum, and the compounds 5b and 5c displayed good activity against Corynespora cassiicola. Theoretical calculation of the compound 5c was carried out with B3LYP/6-31G (d). The full geometry optimization was carried out using 6-31G(d) basis set, and the frontier orbital energy and electrostatic potential were discussed, and the structure-activity relationship was also studied.
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spelling pubmed-43773502015-04-08 Microwave Assisted Synthesis, Antifungal Activity, and DFT Study of Some Novel Triazolinone Derivatives Sun, Na-Bo Jin, Jian-Zhong He, Fang-Yue Biomed Res Int Research Article A series of some novel 1,2,4-triazol-5(4H)-one derivatives were designed and synthesized under microwave irradiation via multistep reaction. The structures of 1,2,4-triazoles were confirmed by (1)H NMR, MS, FTIR, and elemental analysis. The antifungal activities of 1,2,4-triazoles were determined. The antifungal activity results indicated that the compounds 5c, 5f, and 5h exhibited good activity against Pythium ultimum, and the compounds 5b and 5c displayed good activity against Corynespora cassiicola. Theoretical calculation of the compound 5c was carried out with B3LYP/6-31G (d). The full geometry optimization was carried out using 6-31G(d) basis set, and the frontier orbital energy and electrostatic potential were discussed, and the structure-activity relationship was also studied. Hindawi Publishing Corporation 2015 2015-03-12 /pmc/articles/PMC4377350/ /pubmed/25861651 http://dx.doi.org/10.1155/2015/916059 Text en Copyright © 2015 Na-Bo Sun et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Sun, Na-Bo
Jin, Jian-Zhong
He, Fang-Yue
Microwave Assisted Synthesis, Antifungal Activity, and DFT Study of Some Novel Triazolinone Derivatives
title Microwave Assisted Synthesis, Antifungal Activity, and DFT Study of Some Novel Triazolinone Derivatives
title_full Microwave Assisted Synthesis, Antifungal Activity, and DFT Study of Some Novel Triazolinone Derivatives
title_fullStr Microwave Assisted Synthesis, Antifungal Activity, and DFT Study of Some Novel Triazolinone Derivatives
title_full_unstemmed Microwave Assisted Synthesis, Antifungal Activity, and DFT Study of Some Novel Triazolinone Derivatives
title_short Microwave Assisted Synthesis, Antifungal Activity, and DFT Study of Some Novel Triazolinone Derivatives
title_sort microwave assisted synthesis, antifungal activity, and dft study of some novel triazolinone derivatives
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377350/
https://www.ncbi.nlm.nih.gov/pubmed/25861651
http://dx.doi.org/10.1155/2015/916059
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