Russian Chemical Bulletin, volume 67, issue 6, pages 1059-1064
Synthesis, S-alkylation, and fungicidal activity of 4-(benzylideneamino)thioglycolurils
Publication type: Journal Article
Publication date: 2018-06-01
Journal:
Russian Chemical Bulletin
Quartile SCImago
Q3
Quartile WOS
Q3
Impact factor: 1.7
ISSN: 10665285, 15739171
General Chemistry
Abstract
A series of 1,3-disubstituted 4-benzylideneamino-5-thioxohexahydroimidazo[4,5-d]imidazol-2(1H)-ones (thioglycolurils) was synthesized via the reaction of 5,7-disubstituted 3-thioxoperhydroimidazo[4,5-e]-1,2,4-triazin-6-ones with hydroxy-, alkoxy-, and fluorocontaining benzaldehyde derivatives. An alkylation of the obtained thioglycolurils with methyl iodide or 4-bromobenzyl bromide provided the corresponding 6-benzylideneamino-5-alkylsulfanyl-3,3a,6,6a-tetrahydroimidazo[4,5-d]imidazol-2(1H)-ones. The fungicidal activity of some synthesized compounds against pathogens causing diseases of agricultural crops was studied.
Citations by journals
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1
2
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Russian Chemical Bulletin
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Russian Chemical Bulletin
2 publications, 18.18%
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Chemistry of Heterocyclic Compounds
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Chemistry of Heterocyclic Compounds
2 publications, 18.18%
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Synthesis
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Synthesis
1 publication, 9.09%
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Mendeleev Communications
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Mendeleev Communications
1 publication, 9.09%
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New Journal of Chemistry
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New Journal of Chemistry
1 publication, 9.09%
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RSC Advances
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RSC Advances
1 publication, 9.09%
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International Journal of Molecular Sciences
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International Journal of Molecular Sciences
1 publication, 9.09%
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Russian Chemical Reviews
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Russian Chemical Reviews
1 publication, 9.09%
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Organic Process Research and Development
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Organic Process Research and Development
1 publication, 9.09%
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1
2
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Citations by publishers
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1
2
3
4
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Springer Nature
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Springer Nature
4 publications, 36.36%
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Royal Society of Chemistry (RSC)
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Royal Society of Chemistry (RSC)
2 publications, 18.18%
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Thieme
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Thieme
1 publication, 9.09%
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Elsevier
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Elsevier
1 publication, 9.09%
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Multidisciplinary Digital Publishing Institute (MDPI)
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Multidisciplinary Digital Publishing Institute (MDPI)
1 publication, 9.09%
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Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
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Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 9.09%
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American Chemical Society (ACS)
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American Chemical Society (ACS)
1 publication, 9.09%
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1
2
3
4
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- We do not take into account publications that without a DOI.
- Statistics recalculated only for publications connected to researchers, organizations and labs registered on the platform.
- Statistics recalculated weekly.
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Gazieva G. A. et al. Synthesis, S-alkylation, and fungicidal activity of 4-(benzylideneamino)thioglycolurils // Russian Chemical Bulletin. 2018. Vol. 67. No. 6. pp. 1059-1064.
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Gazieva G. A., Nechaeva T. V., Kostikova N. N., Sigay N. V., Serkov S. A., Popkov S. V. Synthesis, S-alkylation, and fungicidal activity of 4-(benzylideneamino)thioglycolurils // Russian Chemical Bulletin. 2018. Vol. 67. No. 6. pp. 1059-1064.
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TY - JOUR
DO - 10.1007/s11172-018-2180-x
UR - https://doi.org/10.1007%2Fs11172-018-2180-x
TI - Synthesis, S-alkylation, and fungicidal activity of 4-(benzylideneamino)thioglycolurils
T2 - Russian Chemical Bulletin
AU - Gazieva, G A
AU - Nechaeva, T. V.
AU - Kostikova, N N
AU - Sigay, N V
AU - Serkov, S A
AU - Popkov, S V
PY - 2018
DA - 2018/06/01 00:00:00
PB - Springer Nature
SP - 1059-1064
IS - 6
VL - 67
SN - 1066-5285
SN - 1573-9171
ER -
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@article{2018_Gazieva,
author = {G A Gazieva and T. V. Nechaeva and N N Kostikova and N V Sigay and S A Serkov and S V Popkov},
title = {Synthesis, S-alkylation, and fungicidal activity of 4-(benzylideneamino)thioglycolurils},
journal = {Russian Chemical Bulletin},
year = {2018},
volume = {67},
publisher = {Springer Nature},
month = {jun},
url = {https://doi.org/10.1007%2Fs11172-018-2180-x},
number = {6},
pages = {1059--1064},
doi = {10.1007/s11172-018-2180-x}
}
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MLA
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Gazieva, G. A., et al. “Synthesis, S-alkylation, and fungicidal activity of 4-(benzylideneamino)thioglycolurils.” Russian Chemical Bulletin, vol. 67, no. 6, Jun. 2018, pp. 1059-1064. https://doi.org/10.1007%2Fs11172-018-2180-x.
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