Russian Chemical Bulletin, volume 59, issue 3, pages 642-646
4,5-Dihydroxyimidazolidin-2-ones in α-ureidoalkylation of N-carboxyalkyl-, N-hydroxyalkyl-, and N-(aminoalkyl)ureas 4.* α-Ureidoalkylation of N-(2-acetylaminoethyl)ureas
Publication type: Journal Article
Publication date: 2010-03-01
Journal:
Russian Chemical Bulletin
Quartile SCImago
Q3
Quartile WOS
Q3
Impact factor: 1.7
ISSN: 10665285, 15739171
General Chemistry
Abstract
Abstractα-Ureidoalkylation of N-(2-acetylammoethyl)ureas with various 4,5-dihydroxyimidazoli-din-2-ones was systematically studied. Novel N-(2-acetylaminoethyl)glycolurils were obtained. Their yields were found to decrease both when moving from l,3-H2-to l,3-Alk2-4,5-dihydroxy-imidazolidin-2-ones and when increasing the size of the substituent at the second N atom in the starting acetylaminoethylurea. The higher yields were achieved with 4,5-diphenyl-4,5-dihydroxyimidazolidin-2-one as the starting compound. 2-(2-Acetylaminoethyl)-4-methylgly-coluril exhibits nootropic activity.
Citations by journals
|
1
2
|
|
|
Russian Chemical Bulletin
|
Russian Chemical Bulletin
2 publications, 25%
|
|
Journal of Heterocyclic Chemistry
|
Journal of Heterocyclic Chemistry
2 publications, 25%
|
|
Mendeleev Communications
|
Mendeleev Communications
1 publication, 12.5%
|
|
Russian Chemical Reviews
|
Russian Chemical Reviews
1 publication, 12.5%
|
|
Russian Journal of Bioorganic Chemistry
|
Russian Journal of Bioorganic Chemistry
1 publication, 12.5%
|
|
Synthesis
|
Synthesis
1 publication, 12.5%
|
|
1
2
|
Citations by publishers
|
1
2
|
|
|
Springer Nature
|
Springer Nature
2 publications, 25%
|
|
Wiley
|
Wiley
2 publications, 25%
|
|
Elsevier
|
Elsevier
1 publication, 12.5%
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 12.5%
|
|
Pleiades Publishing
|
Pleiades Publishing
1 publication, 12.5%
|
|
Thieme
|
Thieme
1 publication, 12.5%
|
|
1
2
|
- 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":[2012,2013,2014,2015,2016,2017,2018,2019,2020],"ids":[0,0,0,0,0,0,0,0,0],"codes":[0,0,0,0,0,0,0,0,0],"imageUrls":["","","","","","","","",""],"datasets":[{"label":"Citations number","data":[2,0,3,0,0,0,2,0,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["25",0,"37.5",0,0,0,"25",0,"12.5"],"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":["Russian Chemical Bulletin","Journal of Heterocyclic Chemistry","Mendeleev Communications","Russian Chemical Reviews","Russian Journal of Bioorganic Chemistry","Synthesis"],"ids":[10918,3189,5294,23802,13594,10934],"codes":[0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp"],"datasets":[{"label":"","data":[2,2,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[25,25,12.5,12.5,12.5,12.5],"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":["Springer Nature","Wiley","Elsevier","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii","Pleiades Publishing","Thieme"],"ids":[8,11,17,9422,101,135],"codes":[0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp"],"datasets":[{"label":"","data":[2,2,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[25,25,12.5,12.5,12.5,12.5],"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
Gazieva G. A. et al. 4,5-Dihydroxyimidazolidin-2-ones in α-ureidoalkylation of N-carboxyalkyl-, N-hydroxyalkyl-, and N-(aminoalkyl)ureas 4.* α-Ureidoalkylation of N-(2-acetylaminoethyl)ureas // Russian Chemical Bulletin. 2010. Vol. 59. No. 3. pp. 642-646.
GOST all authors (up to 50)
Copy
Gazieva G. A., Lozhkin P. V., Baranov V., Kravchenko A. N., Makhova N. N. 4,5-Dihydroxyimidazolidin-2-ones in α-ureidoalkylation of N-carboxyalkyl-, N-hydroxyalkyl-, and N-(aminoalkyl)ureas 4.* α-Ureidoalkylation of N-(2-acetylaminoethyl)ureas // Russian Chemical Bulletin. 2010. Vol. 59. No. 3. pp. 642-646.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1007/s11172-010-0117-0
UR - https://doi.org/10.1007%2Fs11172-010-0117-0
TI - 4,5-Dihydroxyimidazolidin-2-ones in α-ureidoalkylation of N-carboxyalkyl-, N-hydroxyalkyl-, and N-(aminoalkyl)ureas 4.* α-Ureidoalkylation of N-(2-acetylaminoethyl)ureas
T2 - Russian Chemical Bulletin
AU - Gazieva, G A
AU - Lozhkin, P V
AU - Baranov, V.V.
AU - Kravchenko, A N
AU - Makhova, N N
PY - 2010
DA - 2010/03/01 00:00:00
PB - Springer Nature
SP - 642-646
IS - 3
VL - 59
SN - 1066-5285
SN - 1573-9171
ER -
Cite this
BibTex
Copy
@article{2010_Gazieva,
author = {G A Gazieva and P V Lozhkin and V.V. Baranov and A N Kravchenko and N N Makhova},
title = {4,5-Dihydroxyimidazolidin-2-ones in α-ureidoalkylation of N-carboxyalkyl-, N-hydroxyalkyl-, and N-(aminoalkyl)ureas 4.* α-Ureidoalkylation of N-(2-acetylaminoethyl)ureas},
journal = {Russian Chemical Bulletin},
year = {2010},
volume = {59},
publisher = {Springer Nature},
month = {mar},
url = {https://doi.org/10.1007%2Fs11172-010-0117-0},
number = {3},
pages = {642--646},
doi = {10.1007/s11172-010-0117-0}
}
Cite this
MLA
Copy
Gazieva, G. A., et al. “4,5-Dihydroxyimidazolidin-2-ones in α-ureidoalkylation of N-carboxyalkyl-, N-hydroxyalkyl-, and N-(aminoalkyl)ureas 4.* α-Ureidoalkylation of N-(2-acetylaminoethyl)ureas.” Russian Chemical Bulletin, vol. 59, no. 3, Mar. 2010, pp. 642-646. https://doi.org/10.1007%2Fs11172-010-0117-0.