Chemistry of Heterocyclic Compounds, volume 51, issue 8, pages 754-759
An effective synthesis of (1H-1,2,4-triazol-3-yl)furoxans
Publication type: Journal Article
Publication date: 2015-08-01
Journal:
Chemistry of Heterocyclic Compounds
Quartile SCImago
Q3
Quartile WOS
Q3
Impact factor: 1.5
ISSN: 00093122, 15738353
Organic Chemistry
Abstract
A general, simple, and effective method has been developed for the preparation of previously practically unknown (5-R-1Н-1,2,4-triazol-3-yl)furoxans with various substituents at the other carbon atom of furoxan ring, based on condensation of furoxanylamidrazones with electrophilic reagents (cyanogen bromide, acetic and trifluoroacetic anhydrides).
Citations by journals
|
1
2
3
4
5
6
|
|
|
Tetrahedron Letters
|
Tetrahedron Letters
6 publications, 25%
|
|
Chemistry of Heterocyclic Compounds
|
Chemistry of Heterocyclic Compounds
4 publications, 16.67%
|
|
Russian Chemical Bulletin
|
Russian Chemical Bulletin
3 publications, 12.5%
|
|
Mendeleev Communications
|
Mendeleev Communications
2 publications, 8.33%
|
|
RSC Advances
|
RSC Advances
1 publication, 4.17%
|
|
Energetic Materials Frontiers
|
Energetic Materials Frontiers
1 publication, 4.17%
|
|
Frontiers in Chemistry
|
Frontiers in Chemistry
1 publication, 4.17%
|
|
MolBank
|
MolBank
1 publication, 4.17%
|
|
Beilstein Journal of Organic Chemistry
|
Beilstein Journal of Organic Chemistry
1 publication, 4.17%
|
|
Russian Chemical Reviews
|
Russian Chemical Reviews
1 publication, 4.17%
|
|
Inorganica Chimica Acta
|
Inorganica Chimica Acta
1 publication, 4.17%
|
|
New Journal of Chemistry
|
New Journal of Chemistry
1 publication, 4.17%
|
|
Comprehensive Heterocyclic Chemistry IV
|
Comprehensive Heterocyclic Chemistry IV
1 publication, 4.17%
|
|
1
2
3
4
5
6
|
Citations by publishers
|
2
4
6
8
10
12
|
|
|
Elsevier
|
Elsevier
11 publications, 45.83%
|
|
Springer Nature
|
Springer Nature
7 publications, 29.17%
|
|
Royal Society of Chemistry (RSC)
|
Royal Society of Chemistry (RSC)
2 publications, 8.33%
|
|
Frontiers Media S.A.
|
Frontiers Media S.A.
1 publication, 4.17%
|
|
Multidisciplinary Digital Publishing Institute (MDPI)
|
Multidisciplinary Digital Publishing Institute (MDPI)
1 publication, 4.17%
|
|
Beilstein-Institut
|
Beilstein-Institut
1 publication, 4.17%
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 4.17%
|
|
2
4
6
8
10
12
|
- 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":[2015,2016,2017,2018,2019,2020,2021,2022],"ids":[0,0,0,0,0,0,0,0],"codes":[0,0,0,0,0,0,0,0],"imageUrls":["","","","","","","",""],"datasets":[{"label":"Citations number","data":[1,7,4,2,4,1,0,5],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["4.17","29.17","16.67","8.33","16.67","4.17",0,"20.83"],"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":["Tetrahedron Letters","Chemistry of Heterocyclic Compounds","Russian Chemical Bulletin","Mendeleev Communications","RSC Advances","Energetic Materials Frontiers","Frontiers in Chemistry","MolBank","Beilstein Journal of Organic Chemistry","Russian Chemical Reviews","Inorganica Chimica Acta","New Journal of Chemistry","Comprehensive Heterocyclic Chemistry IV"],"ids":[6133,16828,10918,5294,3100,26280,6407,20017,21928,23802,1406,1404,62335],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/4QWA67eqfcfyOiA8Wk7YnqroHFqQbTsmDJUYTCTg_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp"],"datasets":[{"label":"","data":[6,4,3,2,1,1,1,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[25,16.67,12.5,8.33,4.17,4.17,4.17,4.17,4.17,4.17,4.17,4.17,4.17],"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","Springer Nature","Royal Society of Chemistry (RSC)","Frontiers Media S.A.","Multidisciplinary Digital Publishing Institute (MDPI)","Beilstein-Institut","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii"],"ids":[17,8,123,208,202,6139,9422],"codes":[0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/4QWA67eqfcfyOiA8Wk7YnqroHFqQbTsmDJUYTCTg_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[11,7,2,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[45.83,29.17,8.33,4.17,4.17,4.17,4.17],"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
Fershtat L. L. et al. An effective synthesis of (1H-1,2,4-triazol-3-yl)furoxans // Chemistry of Heterocyclic Compounds. 2015. Vol. 51. No. 8. pp. 754-759.
GOST all authors (up to 50)
Copy
Fershtat L. L., Epishina M. A., Ovchinnikov I. V., Kachala V. V., Makhova N. N. An effective synthesis of (1H-1,2,4-triazol-3-yl)furoxans // Chemistry of Heterocyclic Compounds. 2015. Vol. 51. No. 8. pp. 754-759.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1007/s10593-015-1771-9
UR - https://doi.org/10.1007%2Fs10593-015-1771-9
TI - An effective synthesis of (1H-1,2,4-triazol-3-yl)furoxans
T2 - Chemistry of Heterocyclic Compounds
AU - Fershtat, Leonid L
AU - Epishina, Margarita A.
AU - Ovchinnikov, Igor V.
AU - Kachala, Vadim V.
AU - Makhova, Nina N
PY - 2015
DA - 2015/08/01 00:00:00
PB - Springer Nature
SP - 754-759
IS - 8
VL - 51
SN - 0009-3122
SN - 1573-8353
ER -
Cite this
BibTex
Copy
@article{2015_Fershtat,
author = {Leonid L Fershtat and Margarita A. Epishina and Igor V. Ovchinnikov and Vadim V. Kachala and Nina N Makhova},
title = {An effective synthesis of (1H-1,2,4-triazol-3-yl)furoxans},
journal = {Chemistry of Heterocyclic Compounds},
year = {2015},
volume = {51},
publisher = {Springer Nature},
month = {aug},
url = {https://doi.org/10.1007%2Fs10593-015-1771-9},
number = {8},
pages = {754--759},
doi = {10.1007/s10593-015-1771-9}
}
Cite this
MLA
Copy
Fershtat, Leonid L., et al. “An effective synthesis of (1H-1,2,4-triazol-3-yl)furoxans.” Chemistry of Heterocyclic Compounds, vol. 51, no. 8, Aug. 2015, pp. 754-759. https://doi.org/10.1007%2Fs10593-015-1771-9.