Russian Chemical Bulletin, volume 57, issue 8, pages 1760-1764
Glycolurils in α-ureido- and α-aminoalkylation reactions : 22.α -Ureidoalkylation of ureas with N-(hydroxymethyl)glycolurils
Publication type: Journal Article
Publication date: 2008-08-01
Journal:
Russian Chemical Bulletin
Quartile SCImago
Q3
Quartile WOS
Q3
Impact factor: 1.7
ISSN: 10665285, 15739171
General Chemistry
Abstract
Abstractα-Ureidoalkylation of 1,3- and 1,1-dimethylureas with 2-(hydroxymethyl)-, 2,6- and 2,8-di(hydroxymethyl)-, and 2,4,6,8-tetra(hydroxymethyl)glycolurils gave novel bi-, tri-, tetra-, and pentacyclic fused systems combining the glycoluril and urea fragments.
Citations by journals
1
2
|
|
Mendeleev Communications
|
Mendeleev Communications
2 publications, 25%
|
Chemistry of Heterocyclic Compounds
|
Chemistry of Heterocyclic Compounds
2 publications, 25%
|
Russian Chemical Reviews
|
Russian Chemical Reviews
1 publication, 12.5%
|
ChemInform
|
ChemInform
1 publication, 12.5%
|
Russian Journal of General Chemistry
|
Russian Journal of General Chemistry
1 publication, 12.5%
|
Journal of Saudi Chemical Society
|
Journal of Saudi Chemical Society
1 publication, 12.5%
|
1
2
|
Citations by publishers
1
2
|
|
Elsevier
|
Elsevier
2 publications, 25%
|
Springer Nature
|
Springer Nature
2 publications, 25%
|
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%
|
Wiley
|
Wiley
1 publication, 12.5%
|
Pleiades Publishing
|
Pleiades Publishing
1 publication, 12.5%
|
King Saud University
|
King Saud University
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":[2010,2011,2012,2013,2014,2015,2016,2017,2018,2019,2020,2021,2022,2023],"ids":[0,0,0,0,0,0,0,0,0,0,0,0,0,0],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["","","","","","","","","","","","","",""],"datasets":[{"label":"Citations number","data":[1,0,0,0,1,1,1,0,0,0,2,1,0,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["12.5",0,0,0,"12.5","12.5","12.5",0,0,0,"25","12.5",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":["Mendeleev Communications","Chemistry of Heterocyclic Compounds","Russian Chemical Reviews","ChemInform","Russian Journal of General Chemistry","Journal of Saudi Chemical Society"],"ids":[5294,16828,23802,25372,13581,19515],"codes":[0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp","\/storage\/images\/resized\/9z7b0TQJNgUxZHYXLrTmbnjJn9y5iq56Wxtqb1Lv_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":["Elsevier","Springer Nature","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii","Wiley","Pleiades Publishing","King Saud University"],"ids":[17,8,9422,11,101,171],"codes":[0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp","\/storage\/images\/resized\/9z7b0TQJNgUxZHYXLrTmbnjJn9y5iq56Wxtqb1Lv_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
Kravchenko A. N. et al. Glycolurils in α-ureido- and α-aminoalkylation reactions : 22.α -Ureidoalkylation of ureas with N-(hydroxymethyl)glycolurils // Russian Chemical Bulletin. 2008. Vol. 57. No. 8. pp. 1760-1764.
GOST all authors (up to 50)
Copy
Kravchenko A. N., Gazieva G. A., Kolotyrkina N. G., Makhova N. N. Glycolurils in α-ureido- and α-aminoalkylation reactions : 22.α -Ureidoalkylation of ureas with N-(hydroxymethyl)glycolurils // Russian Chemical Bulletin. 2008. Vol. 57. No. 8. pp. 1760-1764.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1007/s11172-008-0233-2
UR - https://doi.org/10.1007%2Fs11172-008-0233-2
TI - Glycolurils in α-ureido- and α-aminoalkylation reactions : 22.α -Ureidoalkylation of ureas with N-(hydroxymethyl)glycolurils
T2 - Russian Chemical Bulletin
AU - Kravchenko, A N
AU - Gazieva, G A
AU - Kolotyrkina, N G
AU - Makhova, N N
PY - 2008
DA - 2008/08/01 00:00:00
PB - Springer Nature
SP - 1760-1764
IS - 8
VL - 57
SN - 1066-5285
SN - 1573-9171
ER -
Cite this
BibTex
Copy
@article{2008_Kravchenko,
author = {A N Kravchenko and G A Gazieva and N G Kolotyrkina and N N Makhova},
title = {Glycolurils in α-ureido- and α-aminoalkylation reactions : 22.α -Ureidoalkylation of ureas with N-(hydroxymethyl)glycolurils},
journal = {Russian Chemical Bulletin},
year = {2008},
volume = {57},
publisher = {Springer Nature},
month = {aug},
url = {https://doi.org/10.1007%2Fs11172-008-0233-2},
number = {8},
pages = {1760--1764},
doi = {10.1007/s11172-008-0233-2}
}
Cite this
MLA
Copy
Kravchenko, A. N., et al. “Glycolurils in α-ureido- and α-aminoalkylation reactions : 22.α -Ureidoalkylation of ureas with N-(hydroxymethyl)glycolurils.” Russian Chemical Bulletin, vol. 57, no. 8, Aug. 2008, pp. 1760-1764. https://doi.org/10.1007%2Fs11172-008-0233-2.
Profiles