Russian Journal of Organic Chemistry, volume 54, issue 10, pages 1515-1518
Hetero-Diels–Alder Reaction of Aroylpyrrolo[1,2-a]quinoxalinetriones with Styrene
Publication type: Journal Article
Publication date: 2018-10-01
Journal:
Russian Journal of Organic Chemistry
Quartile SCImago
Q4
Quartile WOS
Q4
Impact factor: 0.8
ISSN: 10704280, 16083393
Organic Chemistry
Abstract
Hetero-Diels–Alder reaction of 3-aroylpyrrolo[1,2-a]quinoxaline-1,2,4(5H)-triones with styrene afforded diastereoisomeric (5R*,6aR*)- and (5S*,6aR*)-3,5-diaryl-5,6-dihydropyrano[4′,3′:2,3]pyrrolo[1,2-a]-quinoxaline-1,2,7(8H)-triones.
Citations by journals
|
1
|
|
|
Tetrahedron Letters
|
Tetrahedron Letters
1 publication, 25%
|
|
Chemistry of Heterocyclic Compounds
|
Chemistry of Heterocyclic Compounds
1 publication, 25%
|
|
ChemistrySelect
|
ChemistrySelect
1 publication, 25%
|
|
Beilstein Journal of Organic Chemistry
|
Beilstein Journal of Organic Chemistry
1 publication, 25%
|
|
1
|
Citations by publishers
|
1
|
|
|
Elsevier
|
Elsevier
1 publication, 25%
|
|
Springer Nature
|
Springer Nature
1 publication, 25%
|
|
Wiley
|
Wiley
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":[2020,2021,2022],"ids":[0,0,0],"codes":[0,0,0],"imageUrls":["","",""],"datasets":[{"label":"Citations number","data":[1,2,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6"],"percentage":["25","50","25"],"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","ChemistrySelect","Beilstein Journal of Organic Chemistry"],"ids":[6133,16828,8021,21928],"codes":[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\/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":["Elsevier","Springer Nature","Wiley","Beilstein-Institut"],"ids":[17,8,11,6139],"codes":[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\/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
Kasatkina S. O. et al. Hetero-Diels–Alder Reaction of Aroylpyrrolo[1,2-a]quinoxalinetriones with Styrene // Russian Journal of Organic Chemistry. 2018. Vol. 54. No. 10. pp. 1515-1518.
GOST all authors (up to 50)
Copy
Kasatkina S. O., Stepanova E. E., Dmitriev M. V., Maslivets A. N. Hetero-Diels–Alder Reaction of Aroylpyrrolo[1,2-a]quinoxalinetriones with Styrene // Russian Journal of Organic Chemistry. 2018. Vol. 54. No. 10. pp. 1515-1518.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1134/S1070428018100135
UR - https://doi.org/10.1134%2FS1070428018100135
TI - Hetero-Diels–Alder Reaction of Aroylpyrrolo[1,2-a]quinoxalinetriones with Styrene
T2 - Russian Journal of Organic Chemistry
AU - Kasatkina, S O
AU - Stepanova, E E
AU - Dmitriev, M V
AU - Maslivets, A N
PY - 2018
DA - 2018/10/01 00:00:00
PB - Pleiades Publishing
SP - 1515-1518
IS - 10
VL - 54
SN - 1070-4280
SN - 1608-3393
ER -
Cite this
BibTex
Copy
@article{2018_Kasatkina,
author = {S O Kasatkina and E E Stepanova and M V Dmitriev and A N Maslivets},
title = {Hetero-Diels–Alder Reaction of Aroylpyrrolo[1,2-a]quinoxalinetriones with Styrene},
journal = {Russian Journal of Organic Chemistry},
year = {2018},
volume = {54},
publisher = {Pleiades Publishing},
month = {oct},
url = {https://doi.org/10.1134%2FS1070428018100135},
number = {10},
pages = {1515--1518},
doi = {10.1134/S1070428018100135}
}
Cite this
MLA
Copy
Kasatkina, S. O., et al. “Hetero-Diels–Alder Reaction of Aroylpyrrolo[1,2-a]quinoxalinetriones with Styrene.” Russian Journal of Organic Chemistry, vol. 54, no. 10, Oct. 2018, pp. 1515-1518. https://doi.org/10.1134%2FS1070428018100135.