Open Access
Arkivoc, volume 53, issue 8, pages 849-851
Lewis acid-catalyzed Wolff cyclocondensation in the synthesis of (1H-1,2,3-triazolyl)furoxans
Publication type: Journal Article
Publication date: 2017-05-21
Organic Chemistry
Abstract
Novel regioselective approach to the synthesis of (1H-1,2,3-triazol-1-yl)furoxans based on Lewis acid-catalyzed Wolff cyclocondensation of aminofuroxans with diazo-β-dicarbonyl compounds has been developed. This approach allows to involve aminofuroxans as substrates which are very weak nucleophiles and usually do not participate in reactions with common electrophiles.
Citations by journals
|
1
2
3
|
|
|
Tetrahedron Letters
|
Tetrahedron Letters
3 publications, 30%
|
|
Mendeleev Communications
|
Mendeleev Communications
2 publications, 20%
|
|
Chemistry of Heterocyclic Compounds
|
Chemistry of Heterocyclic Compounds
1 publication, 10%
|
|
Molecules
|
Molecules
1 publication, 10%
|
|
European Journal of Organic Chemistry
|
European Journal of Organic Chemistry
1 publication, 10%
|
|
Dalton Transactions
|
Dalton Transactions
1 publication, 10%
|
|
Comprehensive Heterocyclic Chemistry IV
|
Comprehensive Heterocyclic Chemistry IV
1 publication, 10%
|
|
1
2
3
|
Citations by publishers
|
1
2
3
4
5
6
|
|
|
Elsevier
|
Elsevier
6 publications, 60%
|
|
Springer Nature
|
Springer Nature
1 publication, 10%
|
|
Multidisciplinary Digital Publishing Institute (MDPI)
|
Multidisciplinary Digital Publishing Institute (MDPI)
1 publication, 10%
|
|
Wiley
|
Wiley
1 publication, 10%
|
|
Royal Society of Chemistry (RSC)
|
Royal Society of Chemistry (RSC)
1 publication, 10%
|
|
1
2
3
4
5
6
|
- 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],"ids":[0,0,0,0,0,0,0],"codes":[0,0,0,0,0,0,0],"imageUrls":["","","","","","",""],"datasets":[{"label":"Citations number","data":[3,2,2,0,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["30","20","20",0,"10","10","10"],"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","Mendeleev Communications","Chemistry of Heterocyclic Compounds","Molecules","European Journal of Organic Chemistry","Dalton Transactions","Comprehensive Heterocyclic Chemistry IV"],"ids":[6133,5294,16828,1770,19472,8473,62335],"codes":[0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp"],"datasets":[{"label":"","data":[3,2,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[30,20,10,10,10,10,10],"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","Multidisciplinary Digital Publishing Institute (MDPI)","Wiley","Royal Society of Chemistry (RSC)"],"ids":[17,8,202,11,123],"codes":[0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp"],"datasets":[{"label":"","data":[6,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[60,10,10,10,10],"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. Lewis acid-catalyzed Wolff cyclocondensation in the synthesis of (1H-1,2,3-triazolyl)furoxans // Arkivoc. 2017. Vol. 53. No. 8. pp. 849-851.
GOST all authors (up to 50)
Copy
Fershtat L. L., Radzhabov M. R., Romanova A. A., Ananyev I. V., Makhova N. N. Lewis acid-catalyzed Wolff cyclocondensation in the synthesis of (1H-1,2,3-triazolyl)furoxans // Arkivoc. 2017. Vol. 53. No. 8. pp. 849-851.
Cite this
RIS
Copy
TY - JOUR
DO - 10.24820/ark.5550190.p010.070
UR - https://doi.org/10.24820%2Fark.5550190.p010.070
TI - Lewis acid-catalyzed Wolff cyclocondensation in the synthesis of (1H-1,2,3-triazolyl)furoxans
T2 - Arkivoc
AU - Fershtat, Leonid L
AU - Radzhabov, Maxim R
AU - Romanova, Anna A
AU - Ananyev, Ivan V.
AU - Makhova, Nina N
PY - 2017
DA - 2017/05/21 00:00:00
PB - Arkat USA
SP - 849-851
IS - 8
VL - 53
SN - 1551-7004
SN - 1551-7012
ER -
Cite this
BibTex
Copy
@article{2017_Fershtat,
author = {Leonid L Fershtat and Maxim R Radzhabov and Anna A Romanova and Ivan V. Ananyev and Nina N Makhova},
title = {Lewis acid-catalyzed Wolff cyclocondensation in the synthesis of (1H-1,2,3-triazolyl)furoxans},
journal = {Arkivoc},
year = {2017},
volume = {53},
publisher = {Arkat USA},
month = {may},
url = {https://doi.org/10.24820%2Fark.5550190.p010.070},
number = {8},
pages = {849--851},
doi = {10.24820/ark.5550190.p010.070}
}
Cite this
MLA
Copy
Fershtat, Leonid L., et al. “Lewis acid-catalyzed Wolff cyclocondensation in the synthesis of (1H-1,2,3-triazolyl)furoxans.” Arkivoc, vol. 53, no. 8, May. 2017, pp. 849-851. https://doi.org/10.24820%2Fark.5550190.p010.070.
Profiles