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Synthesis and study of the antifungal activity of 1-(2-cyanophenyl)-3-heterylureas. / Dunaeva, Kristina; Baratova, Daria; Kalinina, Tatiana и др.
в: E3S Web of Conferences, Том 474, 03008, 01.01.2024.

Результаты исследований: Вклад в журналМатериалы конференцииРецензирование

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Dunaeva K, Baratova D, Kalinina T, Glukhareva T. Synthesis and study of the antifungal activity of 1-(2-cyanophenyl)-3-heterylureas. E3S Web of Conferences. 2024 янв. 1;474:03008. doi: 10.1051/e3sconf/202447403008

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@article{ad94dc805db241dbb83d5799ee879667,
title = "Synthesis and study of the antifungal activity of 1-(2-cyanophenyl)-3-heterylureas",
abstract = "In the treatment and prevention of fungal infections of plants, along with fungicides, inducers of systemic plant resistance, also called elicitors, have become particularly important in recent years. In this work, a method was developed for the synthesis of new 3,4-dichloroisothiazol-5-yl and 4-methyl-1,2,3-thiadiazol-5-yl ureas 1,2, containing a 2-cyanophenyl substituent, structurally similar to a known synthetic elicitors isotianil and tiadinil. The protective properties of the obtained compounds on cucumber and pepper leaves infected with B. cinerea, as well as their fungicidal properties against B. cinerea, were studied. It has been established that disubstituted ureas 1,2 exhibit very low fungicidal activity against this fungus, about 11%. At the same time, study on plant leaves showed that compound 2 effectively inhibited the development of gray mold on both cucumber and pepper leaves with an inhibition rate of more than 90%, which was similar to tiadinil. Compound 1 was effective only on cucumber leaves (96.50±0.01%). Isotianil in the experiment showed an average degree of protection - 62.48±1.04% on cucumber leaves and 56.50±1.29% on pepper leaves. {\textcopyright} The Authors, published by EDP Sciences. This is an open access article distributed under the terms of the Creative Commons Attribution License 4.0 (https://creativecommons.org/licenses/by/4.0/).",
author = "Kristina Dunaeva and Daria Baratova and Tatiana Kalinina and Tatiana Glukhareva",
note = "This research was supported by the Russian Science Foundation and Government of Sverdlovsk region, Joint Grant No 22-26-20124, https://rscf.ru/en/project/22-26-20124/ (accessed on 30 October 2023).; 10th International Annual Conference on Industrial Technologies and Engineering, ICITE 2023 ; Conference date: 09-11-2023",
year = "2024",
month = jan,
day = "1",
doi = "10.1051/e3sconf/202447403008",
language = "English",
volume = "474",
journal = "E3S Web of Conferences",
issn = "2261-236X",
publisher = "EDP Sciences",

}

RIS

TY - JOUR

T1 - Synthesis and study of the antifungal activity of 1-(2-cyanophenyl)-3-heterylureas

AU - Dunaeva, Kristina

AU - Baratova, Daria

AU - Kalinina, Tatiana

AU - Glukhareva, Tatiana

N1 - This research was supported by the Russian Science Foundation and Government of Sverdlovsk region, Joint Grant No 22-26-20124, https://rscf.ru/en/project/22-26-20124/ (accessed on 30 October 2023).

PY - 2024/1/1

Y1 - 2024/1/1

N2 - In the treatment and prevention of fungal infections of plants, along with fungicides, inducers of systemic plant resistance, also called elicitors, have become particularly important in recent years. In this work, a method was developed for the synthesis of new 3,4-dichloroisothiazol-5-yl and 4-methyl-1,2,3-thiadiazol-5-yl ureas 1,2, containing a 2-cyanophenyl substituent, structurally similar to a known synthetic elicitors isotianil and tiadinil. The protective properties of the obtained compounds on cucumber and pepper leaves infected with B. cinerea, as well as their fungicidal properties against B. cinerea, were studied. It has been established that disubstituted ureas 1,2 exhibit very low fungicidal activity against this fungus, about 11%. At the same time, study on plant leaves showed that compound 2 effectively inhibited the development of gray mold on both cucumber and pepper leaves with an inhibition rate of more than 90%, which was similar to tiadinil. Compound 1 was effective only on cucumber leaves (96.50±0.01%). Isotianil in the experiment showed an average degree of protection - 62.48±1.04% on cucumber leaves and 56.50±1.29% on pepper leaves. © The Authors, published by EDP Sciences. This is an open access article distributed under the terms of the Creative Commons Attribution License 4.0 (https://creativecommons.org/licenses/by/4.0/).

AB - In the treatment and prevention of fungal infections of plants, along with fungicides, inducers of systemic plant resistance, also called elicitors, have become particularly important in recent years. In this work, a method was developed for the synthesis of new 3,4-dichloroisothiazol-5-yl and 4-methyl-1,2,3-thiadiazol-5-yl ureas 1,2, containing a 2-cyanophenyl substituent, structurally similar to a known synthetic elicitors isotianil and tiadinil. The protective properties of the obtained compounds on cucumber and pepper leaves infected with B. cinerea, as well as their fungicidal properties against B. cinerea, were studied. It has been established that disubstituted ureas 1,2 exhibit very low fungicidal activity against this fungus, about 11%. At the same time, study on plant leaves showed that compound 2 effectively inhibited the development of gray mold on both cucumber and pepper leaves with an inhibition rate of more than 90%, which was similar to tiadinil. Compound 1 was effective only on cucumber leaves (96.50±0.01%). Isotianil in the experiment showed an average degree of protection - 62.48±1.04% on cucumber leaves and 56.50±1.29% on pepper leaves. © The Authors, published by EDP Sciences. This is an open access article distributed under the terms of the Creative Commons Attribution License 4.0 (https://creativecommons.org/licenses/by/4.0/).

UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85183306472

U2 - 10.1051/e3sconf/202447403008

DO - 10.1051/e3sconf/202447403008

M3 - Conference article

VL - 474

JO - E3S Web of Conferences

JF - E3S Web of Conferences

SN - 2261-236X

M1 - 03008

T2 - 10th International Annual Conference on Industrial Technologies and Engineering, ICITE 2023

Y2 - 9 November 2023

ER -

ID: 52304021