Open Access
Arkivoc, volume 2017, issue 3, pages 250-268
Synthesis, structural characterization and cytotoxic activity of heterocyclic compounds containing the furoxan ring
Publication type: Journal Article
Publication date: 2017-08-07
Organic Chemistry
Abstract
A direct approach to the synthesis of previously unknown 1H-1,2,3-triazolylfuroxans, involving nucleophilic substitution of the nitro group in nitrofuroxans followed by catalytic [3+2] cycloaddition of intermediate azidofuroxans to 1,3-ketoesters, is reported. The scope of the triazolylfuroxans was additionally diversified through a number of transformations of the functional groups attached to the 1,2,3-triazole ring. The cytotoxic activity of the newly synthesized triazolylfuroxans and of previously reported hetarylfuroxans was studied. The NO-donor capability of selected synthesized hetarylfuroxans was measured by the Griess reaction using a spectrophotometric technique.
Citations by journals
1
2
3
4
5
6
7
8
9
|
|
Mendeleev Communications
|
Mendeleev Communications
9 publications, 40.91%
|
Tetrahedron Letters
|
Tetrahedron Letters
4 publications, 18.18%
|
International Journal of Molecular Sciences
|
International Journal of Molecular Sciences
2 publications, 9.09%
|
European Journal of Organic Chemistry
|
European Journal of Organic Chemistry
1 publication, 4.55%
|
ChemPhotoChem
|
ChemPhotoChem
1 publication, 4.55%
|
Russian Chemical Bulletin
|
Russian Chemical Bulletin
1 publication, 4.55%
|
Computational and Structural Biotechnology Journal
|
Computational and Structural Biotechnology Journal
1 publication, 4.55%
|
Journal of Heterocyclic Chemistry
|
Journal of Heterocyclic Chemistry
1 publication, 4.55%
|
Comprehensive Heterocyclic Chemistry IV
|
Comprehensive Heterocyclic Chemistry IV
1 publication, 4.55%
|
Molecules
|
Molecules
1 publication, 4.55%
|
1
2
3
4
5
6
7
8
9
|
Citations by publishers
2
4
6
8
10
12
14
16
|
|
Elsevier
|
Elsevier
15 publications, 68.18%
|
Wiley
|
Wiley
3 publications, 13.64%
|
Multidisciplinary Digital Publishing Institute (MDPI)
|
Multidisciplinary Digital Publishing Institute (MDPI)
3 publications, 13.64%
|
Springer Nature
|
Springer Nature
1 publication, 4.55%
|
2
4
6
8
10
12
14
16
|
- 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.
{"yearsCitations":{"type":"bar","data":{"show":true,"labels":[2017,2018,2019,2020,2021,2022,2023,2024],"ids":[0,0,0,0,0,0,0,0],"codes":[0,0,0,0,0,0,0,0],"imageUrls":["","","","","","","",""],"datasets":[{"label":"Citations number","data":[3,6,2,2,3,2,3,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["13.64","27.27","9.09","9.09","13.64","9.09","13.64","4.55"],"barThickness":null}]},"options":{"indexAxis":"x","maintainAspectRatio":true,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"}},"x":{"ticks":{"stepSize":1,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"}}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Citations per year","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}},"journals":{"type":"bar","data":{"show":true,"labels":["Mendeleev Communications","Tetrahedron Letters","International Journal of Molecular Sciences","European Journal of Organic Chemistry","ChemPhotoChem","Russian Chemical Bulletin","Computational and Structural Biotechnology Journal","Journal of Heterocyclic Chemistry","Comprehensive Heterocyclic Chemistry IV","Molecules"],"ids":[5294,6133,14627,19472,25567,10918,4268,3189,62335,1770],"codes":[0,0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp"],"datasets":[{"label":"","data":[9,4,2,1,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[40.91,18.18,9.09,4.55,4.55,4.55,4.55,4.55,4.55,4.55],"barThickness":13}]},"options":{"indexAxis":"y","maintainAspectRatio":false,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"}},"x":{"ticks":{"stepSize":null,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"}}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Journals","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}},"publishers":{"type":"bar","data":{"show":true,"labels":["Elsevier","Wiley","Multidisciplinary Digital Publishing Institute (MDPI)","Springer Nature"],"ids":[17,11,202,8],"codes":[0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp"],"datasets":[{"label":"","data":[15,3,3,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[68.18,13.64,13.64,4.55],"barThickness":13}]},"options":{"indexAxis":"y","maintainAspectRatio":false,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"}},"x":{"ticks":{"stepSize":null,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"}}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Publishers","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}}}
Metrics
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
Kulikov A. S. et al. Synthesis, structural characterization and cytotoxic activity of heterocyclic compounds containing the furoxan ring // Arkivoc. 2017. Vol. 2017. No. 3. pp. 250-268.
GOST all authors (up to 50)
Copy
Kulikov A. S., Larin A. A., Fershtat L. L., Anikina L. V., Pukhov S. A., Klochkov S. G., Struchkova M. I., Romanova A. A., Ananyev I. V., Makhova N. N. Synthesis, structural characterization and cytotoxic activity of heterocyclic compounds containing the furoxan ring // Arkivoc. 2017. Vol. 2017. No. 3. pp. 250-268.
Cite this
RIS
Copy
TY - JOUR
DO - 10.24820/ark.5550190.p010.229
UR - https://doi.org/10.24820%2Fark.5550190.p010.229
TI - Synthesis, structural characterization and cytotoxic activity of heterocyclic compounds containing the furoxan ring
T2 - Arkivoc
AU - Kulikov, Alexander S.
AU - Larin, Alexander A
AU - Fershtat, Leonid L
AU - Anikina, Lada V
AU - Pukhov, Sergey A.
AU - Klochkov, Sergey G.
AU - Struchkova, Marina I.
AU - Romanova, Anna A
AU - Ananyev, Ivan V.
AU - Makhova, Nina N
PY - 2017
DA - 2017/08/07 00:00:00
PB - Arkat USA
SP - 250-268
IS - 3
VL - 2017
SN - 1551-7004
SN - 1551-7012
ER -
Cite this
BibTex
Copy
@article{2017_Kulikov,
author = {Alexander S. Kulikov and Alexander A Larin and Leonid L Fershtat and Lada V Anikina and Sergey A. Pukhov and Sergey G. Klochkov and Marina I. Struchkova and Anna A Romanova and Ivan V. Ananyev and Nina N Makhova},
title = {Synthesis, structural characterization and cytotoxic activity of heterocyclic compounds containing the furoxan ring},
journal = {Arkivoc},
year = {2017},
volume = {2017},
publisher = {Arkat USA},
month = {aug},
url = {https://doi.org/10.24820%2Fark.5550190.p010.229},
number = {3},
pages = {250--268},
doi = {10.24820/ark.5550190.p010.229}
}
Cite this
MLA
Copy
Kulikov, Alexander S., et al. “Synthesis, structural characterization and cytotoxic activity of heterocyclic compounds containing the furoxan ring.” Arkivoc, vol. 2017, no. 3, Aug. 2017, pp. 250-268. https://doi.org/10.24820%2Fark.5550190.p010.229.