Russian Journal of Organic Chemistry, volume 57, issue 1, pages 32-37
[3+2]-Dipolar Cycloaddition of Nitrones to Pyrroloquinoxalinetriones
Publication type: Journal Article
Publication date: 2021-01-01
Journal:
Russian Journal of Organic Chemistry
Quartile SCImago
Q4
Quartile WOS
Q4
Impact factor: 0.8
ISSN: 10704280, 16083393
Organic Chemistry
Abstract
Abstract [3+2]-Dipolar cycloaddition of diarylnitrones to substituted pyrroloquinoxalinetriones afforded (2a S *,3 R *,5a S *)-2a-acyl-3,4-diaryl-3,4-dihydro-1 H -[1,2]oxazolo[5′,4′:2,3]pyrrolo[1,2- a ]quinoxaline-1,2,6(2a H ,7 H )-triones that attract interest for medicinal chemistry.
Citations by journals
1
|
|
RSC Advances
|
RSC Advances
1 publication, 25%
|
Chemistry of Heterocyclic Compounds
|
Chemistry of Heterocyclic Compounds
1 publication, 25%
|
Russian Journal of Organic Chemistry
|
Russian Journal of Organic Chemistry
1 publication, 25%
|
Beilstein Journal of Organic Chemistry
|
Beilstein Journal of Organic Chemistry
1 publication, 25%
|
1
|
Citations by publishers
1
|
|
Royal Society of Chemistry (RSC)
|
Royal Society of Chemistry (RSC)
1 publication, 25%
|
Springer Nature
|
Springer Nature
1 publication, 25%
|
Pleiades Publishing
|
Pleiades Publishing
1 publication, 25%
|
Beilstein-Institut
|
Beilstein-Institut
1 publication, 25%
|
1
|
- 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":[2021,2022],"ids":[0,0],"codes":[0,0],"imageUrls":["",""],"datasets":[{"label":"Citations number","data":[1,3],"backgroundColor":["#3B82F6","#3B82F6"],"percentage":["25","75"],"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":["RSC Advances","Chemistry of Heterocyclic Compounds","Russian Journal of Organic Chemistry","Beilstein Journal of Organic Chemistry"],"ids":[3100,16828,5728,21928],"codes":[0,0,0,0],"imageUrls":["\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp"],"datasets":[{"label":"","data":[1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[25,25,25,25],"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":["Royal Society of Chemistry (RSC)","Springer Nature","Pleiades Publishing","Beilstein-Institut"],"ids":[123,8,101,6139],"codes":[0,0,0,0],"imageUrls":["\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp"],"datasets":[{"label":"","data":[1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[25,25,25,25],"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
Stepanova E. E., Dmitriev M. V., Maslivets A. N. [3+2]-Dipolar Cycloaddition of Nitrones to Pyrroloquinoxalinetriones // Russian Journal of Organic Chemistry. 2021. Vol. 57. No. 1. pp. 32-37.
GOST all authors (up to 50)
Copy
Stepanova E. E., Dmitriev M. V., Maslivets A. N. [3+2]-Dipolar Cycloaddition of Nitrones to Pyrroloquinoxalinetriones // Russian Journal of Organic Chemistry. 2021. Vol. 57. No. 1. pp. 32-37.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1134/S107042802101005X
UR - https://doi.org/10.1134%2FS107042802101005X
TI - [3+2]-Dipolar Cycloaddition of Nitrones to Pyrroloquinoxalinetriones
T2 - Russian Journal of Organic Chemistry
AU - Stepanova, E E
AU - Dmitriev, M V
AU - Maslivets, A N
PY - 2021
DA - 2021/01/01 00:00:00
PB - Pleiades Publishing
SP - 32-37
IS - 1
VL - 57
SN - 1070-4280
SN - 1608-3393
ER -
Cite this
BibTex
Copy
@article{2021_Stepanova,
author = {E E Stepanova and M V Dmitriev and A N Maslivets},
title = {[3+2]-Dipolar Cycloaddition of Nitrones to Pyrroloquinoxalinetriones},
journal = {Russian Journal of Organic Chemistry},
year = {2021},
volume = {57},
publisher = {Pleiades Publishing},
month = {jan},
url = {https://doi.org/10.1134%2FS107042802101005X},
number = {1},
pages = {32--37},
doi = {10.1134/S107042802101005X}
}
Cite this
MLA
Copy
Stepanova, E. E., et al. “[3+2]-Dipolar Cycloaddition of Nitrones to Pyrroloquinoxalinetriones.” Russian Journal of Organic Chemistry, vol. 57, no. 1, Jan. 2021, pp. 32-37. https://doi.org/10.1134%2FS107042802101005X.