Open Access
RSC Advances, volume 6, issue 37, pages 31526-31539
Design of hybrid heterocyclic systems with a furoxanylpyridine core via tandem hetero-Diels-Alder/retro-Diels-Alder reactions of (1,2,4-triazin-3-yl)furoxans
Fershtat Leonid L.
1, 2, 3, 4
,
Larin Alexander A
1, 2, 3, 4
,
Epishina Margarita A.
1, 2, 3, 4
,
Ovchinnikov I.V.
1, 2, 3, 4
,
Kulikov Alexander
1, 2, 3, 4
,
Ananyev Ivan V
2, 4, 5, 6
,
Makhova Nina N.
1, 2, 3, 4
2
RUSSIAN ACADEMY OF SCIENCES
3
Moscow
4
RUSSIAN FEDERATION
|
6
119991 Moscow
Publication type: Journal Article
Publication date: 2016-03-22
General Chemistry
General Chemical Engineering
Abstract
Synthetic strategy for the synthesis of hybrid heterocyclic systems with the furoxanylpyridine core based on the tandem hetero-Diels–Alder/retro-Diels–Alder reactions of (1,2,4-triazin-3-yl)furoxans with enamine and norbornadiene has been developed.
Citations by journals
1
2
3
4
5
6
|
|
Tetrahedron Letters
|
Tetrahedron Letters
6 publications, 14.63%
|
Russian Chemical Bulletin
|
Russian Chemical Bulletin
6 publications, 14.63%
|
Mendeleev Communications
|
Mendeleev Communications
6 publications, 14.63%
|
Chemistry of Heterocyclic Compounds
|
Chemistry of Heterocyclic Compounds
3 publications, 7.32%
|
ChemistrySelect
|
ChemistrySelect
2 publications, 4.88%
|
European Journal of Organic Chemistry
|
European Journal of Organic Chemistry
2 publications, 4.88%
|
Advanced Synthesis and Catalysis
|
Advanced Synthesis and Catalysis
1 publication, 2.44%
|
ChemPlusChem
|
ChemPlusChem
1 publication, 2.44%
|
ChemMedChem
|
ChemMedChem
1 publication, 2.44%
|
Journal of Physical Chemistry A
|
Journal of Physical Chemistry A
1 publication, 2.44%
|
Beilstein Journal of Organic Chemistry
|
Beilstein Journal of Organic Chemistry
1 publication, 2.44%
|
Russian Chemical Reviews
|
Russian Chemical Reviews
1 publication, 2.44%
|
Coordination Chemistry Reviews
|
Coordination Chemistry Reviews
1 publication, 2.44%
|
ChemInform
|
ChemInform
1 publication, 2.44%
|
Asian Journal of Organic Chemistry
|
Asian Journal of Organic Chemistry
1 publication, 2.44%
|
Journal of Organic Chemistry
|
Journal of Organic Chemistry
1 publication, 2.44%
|
Organic and Biomolecular Chemistry
|
Organic and Biomolecular Chemistry
1 publication, 2.44%
|
Organic Chemistry Frontiers
|
Organic Chemistry Frontiers
1 publication, 2.44%
|
Progress in Heterocyclic Chemistry
|
Progress in Heterocyclic Chemistry
1 publication, 2.44%
|
Doklady Chemistry
|
Doklady Chemistry
1 publication, 2.44%
|
Comprehensive Heterocyclic Chemistry IV
|
Comprehensive Heterocyclic Chemistry IV
1 publication, 2.44%
|
1
2
3
4
5
6
|
Citations by publishers
2
4
6
8
10
12
14
16
|
|
Elsevier
|
Elsevier
15 publications, 36.59%
|
Springer Nature
|
Springer Nature
9 publications, 21.95%
|
Wiley
|
Wiley
9 publications, 21.95%
|
American Chemical Society (ACS)
|
American Chemical Society (ACS)
2 publications, 4.88%
|
Royal Society of Chemistry (RSC)
|
Royal Society of Chemistry (RSC)
2 publications, 4.88%
|
Beilstein-Institut
|
Beilstein-Institut
1 publication, 2.44%
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 2.44%
|
Pleiades Publishing
|
Pleiades Publishing
1 publication, 2.44%
|
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":[2016,2017,2018,2019,2020,2021,2022,2023],"ids":[0,0,0,0,0,0,0,0],"codes":[0,0,0,0,0,0,0,0],"imageUrls":["","","","","","","",""],"datasets":[{"label":"Citations number","data":[4,12,9,3,4,1,5,3],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["9.76","29.27","21.95","7.32","9.76","2.44","12.2","7.32"],"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","Russian Chemical Bulletin","Mendeleev Communications","Chemistry of Heterocyclic Compounds","ChemistrySelect","European Journal of Organic Chemistry","Advanced Synthesis and Catalysis","ChemPlusChem","ChemMedChem","Journal of Physical Chemistry A","Beilstein Journal of Organic Chemistry","Russian Chemical Reviews","Coordination Chemistry Reviews","ChemInform","Asian Journal of Organic Chemistry","Journal of Organic Chemistry","Organic and Biomolecular Chemistry","Organic Chemistry Frontiers","Progress in Heterocyclic Chemistry","Doklady Chemistry","Comprehensive Heterocyclic Chemistry IV"],"ids":[6133,10918,5294,16828,8021,19472,3906,21067,1430,15255,21928,23802,13437,25372,9409,8697,541,3991,17224,11308,62335],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp"],"datasets":[{"label":"","data":[6,6,6,3,2,2,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[14.63,14.63,14.63,7.32,4.88,4.88,2.44,2.44,2.44,2.44,2.44,2.44,2.44,2.44,2.44,2.44,2.44,2.44,2.44,2.44,2.44],"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","Wiley","American Chemical Society (ACS)","Royal Society of Chemistry (RSC)","Beilstein-Institut","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii","Pleiades Publishing"],"ids":[17,8,11,40,123,6139,9422,101],"codes":[0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp"],"datasets":[{"label":"","data":[15,9,9,2,2,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[36.59,21.95,21.95,4.88,4.88,2.44,2.44,2.44],"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. Design of hybrid heterocyclic systems with a furoxanylpyridine core via tandem hetero-Diels-Alder/retro-Diels-Alder reactions of (1,2,4-triazin-3-yl)furoxans // RSC Advances. 2016. Vol. 6. No. 37. pp. 31526-31539.
GOST all authors (up to 50)
Copy
Fershtat L. L., Larin A. A., Epishina M. A., Ovchinnikov I., Kulikov A., Ananyev I. V., Makhova N. N. Design of hybrid heterocyclic systems with a furoxanylpyridine core via tandem hetero-Diels-Alder/retro-Diels-Alder reactions of (1,2,4-triazin-3-yl)furoxans // RSC Advances. 2016. Vol. 6. No. 37. pp. 31526-31539.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1039/c6ra05110c
UR - https://doi.org/10.1039%2Fc6ra05110c
TI - Design of hybrid heterocyclic systems with a furoxanylpyridine core via tandem hetero-Diels-Alder/retro-Diels-Alder reactions of (1,2,4-triazin-3-yl)furoxans
T2 - RSC Advances
AU - Epishina, Margarita A.
AU - Fershtat, Leonid L.
AU - Larin, Alexander A
AU - Ovchinnikov, I.V.
AU - Kulikov, Alexander
AU - Ananyev, Ivan V
AU - Makhova, Nina N.
PY - 2016
DA - 2016/03/22 00:00:00
PB - Royal Society of Chemistry (RSC)
SP - 31526-31539
IS - 37
VL - 6
SN - 2046-2069
ER -
Cite this
BibTex
Copy
@article{2016_Fershtat
author = {Margarita A. Epishina and Leonid L. Fershtat and Alexander A Larin and I.V. Ovchinnikov and Alexander Kulikov and Ivan V Ananyev and Nina N. Makhova},
title = {Design of hybrid heterocyclic systems with a furoxanylpyridine core via tandem hetero-Diels-Alder/retro-Diels-Alder reactions of (1,2,4-triazin-3-yl)furoxans},
journal = {RSC Advances},
year = {2016},
volume = {6},
publisher = {Royal Society of Chemistry (RSC)},
month = {mar},
url = {https://doi.org/10.1039%2Fc6ra05110c},
number = {37},
pages = {31526--31539},
doi = {10.1039/c6ra05110c}
}
Cite this
MLA
Copy
Fershtat, Leonid L., et al. “Design of hybrid heterocyclic systems with a furoxanylpyridine core via tandem hetero-Diels-Alder/retro-Diels-Alder reactions of (1,2,4-triazin-3-yl)furoxans.” RSC Advances, vol. 6, no. 37, Mar. 2016, pp. 31526-31539. https://doi.org/10.1039%2Fc6ra05110c.