Open Access
Beilstein Journal of Organic Chemistry, volume 15, pages 364-370
Annulation of 1H-pyrrole-2,3-diones by thioacetamide: An approach to 5-azaisatins
Publication type: Journal Article
Publication date: 2019-02-07
Quartile SCImago
Q2
Quartile WOS
Q2
Impact factor: 2.7
ISSN: 18605397
PubMed ID:
30800185
Organic Chemistry
Abstract
A novel approach to 1H-pyrrolo[3,2-c]pyridine-2,3-diones (5-azaisatins) has been developed via an unprecedented annulation of pyrrolo[2,1-c][1,4]benzoxazine-1,2,4-triones by thioacetamide. A new way of C–H functionalization of thioacetamide has been discovered. The reaction proceeds under green catalyst-free conditions.
Citations by journals
|
1
|
|
|
Beilstein Journal of Organic Chemistry
|
Beilstein Journal of Organic Chemistry
1 publication, 33.33%
|
|
ChemistrySelect
|
ChemistrySelect
1 publication, 33.33%
|
|
ACS Applied Nano Materials
|
ACS Applied Nano Materials
1 publication, 33.33%
|
|
1
|
Citations by publishers
|
1
|
|
|
Beilstein-Institut
|
Beilstein-Institut
1 publication, 33.33%
|
|
Wiley
|
Wiley
1 publication, 33.33%
|
|
American Chemical Society (ACS)
|
American Chemical Society (ACS)
1 publication, 33.33%
|
|
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":[2019,2020,2021],"ids":[0,0,0],"codes":[0,0,0],"imageUrls":["","",""],"datasets":[{"label":"Citations number","data":[1,0,2],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6"],"percentage":["33.33",0,"66.67"],"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":["Beilstein Journal of Organic Chemistry","ChemistrySelect","ACS Applied Nano Materials"],"ids":[21928,8021,1600],"codes":[0,0,0],"imageUrls":["\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp"],"datasets":[{"label":"","data":[1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6"],"percentage":[33.33,33.33,33.33],"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":["Beilstein-Institut","Wiley","American Chemical Society (ACS)"],"ids":[6139,11,40],"codes":[0,0,0],"imageUrls":["\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp"],"datasets":[{"label":"","data":[1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6"],"percentage":[33.33,33.33,33.33],"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
Cite this
GOST
Copy
Kobelev A. I. et al. Annulation of 1H-pyrrole-2,3-diones by thioacetamide: An approach to 5-azaisatins // Beilstein Journal of Organic Chemistry. 2019. Vol. 15. pp. 364-370.
GOST all authors (up to 50)
Copy
Kobelev A. I., Khramtsova E. E., Dmitriev M. V., Maslivets A. N., Dmitriev M. V., Maslivets A. N. Annulation of 1H-pyrrole-2,3-diones by thioacetamide: An approach to 5-azaisatins // Beilstein Journal of Organic Chemistry. 2019. Vol. 15. pp. 364-370.
Cite this
RIS
Copy
TY - JOUR
DO - 10.3762/bjoc.15.32
UR - https://doi.org/10.3762%2Fbjoc.15.32
TI - Annulation of 1H-pyrrole-2,3-diones by thioacetamide: An approach to 5-azaisatins
T2 - Beilstein Journal of Organic Chemistry
AU - Kobelev, A I
AU - Khramtsova, Ekaterina E
AU - Dmitriev, Maksim V.
AU - Maslivets, Andrey N.
AU - Dmitriev, Maksim V
AU - Maslivets, Andrey N
PY - 2019
DA - 2019/02/07 00:00:00
PB - Beilstein-Institut
SP - 364-370
VL - 15
PMID - 30800185
SN - 1860-5397
ER -
Cite this
BibTex
Copy
@article{2019_Kobelev,
author = {A I Kobelev and Ekaterina E Khramtsova and Maksim V. Dmitriev and Andrey N. Maslivets and Maksim V Dmitriev and Andrey N Maslivets},
title = {Annulation of 1H-pyrrole-2,3-diones by thioacetamide: An approach to 5-azaisatins},
journal = {Beilstein Journal of Organic Chemistry},
year = {2019},
volume = {15},
publisher = {Beilstein-Institut},
month = {feb},
url = {https://doi.org/10.3762%2Fbjoc.15.32},
pages = {364--370},
doi = {10.3762/bjoc.15.32}
}