Open Access
Synthesis, volume 52, issue 17, pages 2563-2571
Synthesis and Structure of 1-Substituted Semithioglycolurils
Publication type: Journal Article
Publication date: 2020-05-25
Catalysis
Organic Chemistry
Abstract
Two methods for the synthesis of previously unavailable 1-substituted semithioglycolurils were developed. These methods consist of the cyclocondensation of 1-substituted ureas with 4,5-dihydroxy- or 4,5-dimethoxyimidazolidine-2-thione or glyoxal, followed by the reaction of the resulting 1-substituted 4,5-dihydroxyimidazolidine-2-ones with HSCN in a two-step one-pot procedure. Two of the desired semithioglycolurils were obtained as conglomerates.
Citations by journals
|
1
2
3
4
|
|
|
Mendeleev Communications
|
Mendeleev Communications
4 publications, 40%
|
|
Chemistry of Heterocyclic Compounds
|
Chemistry of Heterocyclic Compounds
1 publication, 10%
|
|
Magnetochemistry
|
Magnetochemistry
1 publication, 10%
|
|
Russian Chemical Reviews
|
Russian Chemical Reviews
1 publication, 10%
|
|
Bioorganic and Medicinal Chemistry Letters
|
Bioorganic and Medicinal Chemistry Letters
1 publication, 10%
|
|
Heterocycles
|
Heterocycles
1 publication, 10%
|
|
ChemistrySelect
|
ChemistrySelect
1 publication, 10%
|
|
1
2
3
4
|
Citations by publishers
|
1
2
3
4
5
|
|
|
Elsevier
|
Elsevier
5 publications, 50%
|
|
Springer Nature
|
Springer Nature
1 publication, 10%
|
|
Multidisciplinary Digital Publishing Institute (MDPI)
|
Multidisciplinary Digital Publishing Institute (MDPI)
1 publication, 10%
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 10%
|
|
The Japan Institute of Heterocyclic Chemistry
|
The Japan Institute of Heterocyclic Chemistry
1 publication, 10%
|
|
Wiley
|
Wiley
1 publication, 10%
|
|
1
2
3
4
5
|
- 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":[2021,2022,2023,2024],"ids":[0,0,0,0],"codes":[0,0,0,0],"imageUrls":["","","",""],"datasets":[{"label":"Citations number","data":[3,5,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["30","50","10","10"],"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","Magnetochemistry","Russian Chemical Reviews","Bioorganic and Medicinal Chemistry Letters","Heterocycles","ChemistrySelect"],"ids":[5294,16828,25379,23802,8828,22287,8021],"codes":[0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/SovkqI6gX6to8o5XBnS9RNxEOYVicn7hatkMzrvl_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp"],"datasets":[{"label":"","data":[4,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[40,10,10,10,10,10,10],"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","Multidisciplinary Digital Publishing Institute (MDPI)","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii","The Japan Institute of Heterocyclic Chemistry","Wiley"],"ids":[17,8,202,9422,9411,11],"codes":[0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp","\/storage\/images\/resized\/SovkqI6gX6to8o5XBnS9RNxEOYVicn7hatkMzrvl_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp"],"datasets":[{"label":"","data":[5,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[50,10,10,10,10,10],"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
Baranov P. G. et al. Synthesis and Structure of 1-Substituted Semithioglycolurils // Synthesis. 2020. Vol. 52. No. 17. pp. 2563-2571.
GOST all authors (up to 50)
Copy
Baranov P. G., Galochkin A. A., Nelyubina Y. V., Kravchenko A. N., Makhova N. N. Synthesis and Structure of 1-Substituted Semithioglycolurils // Synthesis. 2020. Vol. 52. No. 17. pp. 2563-2571.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1055/s-0040-1707391
UR - https://doi.org/10.1055%2Fs-0040-1707391
TI - Synthesis and Structure of 1-Substituted Semithioglycolurils
T2 - Synthesis
AU - Baranov, Pavel G.
AU - Galochkin, Anton A
AU - Nelyubina, Yulia V.
AU - Kravchenko, Angelina N
AU - Makhova, Nina N
PY - 2020
DA - 2020/05/25 00:00:00
PB - Thieme
SP - 2563-2571
IS - 17
VL - 52
SN - 0039-7881
SN - 1437-210X
ER -
Cite this
BibTex
Copy
@article{2020_Baranov,
author = {Pavel G. Baranov and Anton A Galochkin and Yulia V. Nelyubina and Angelina N Kravchenko and Nina N Makhova},
title = {Synthesis and Structure of 1-Substituted Semithioglycolurils},
journal = {Synthesis},
year = {2020},
volume = {52},
publisher = {Thieme},
month = {may},
url = {https://doi.org/10.1055%2Fs-0040-1707391},
number = {17},
pages = {2563--2571},
doi = {10.1055/s-0040-1707391}
}
Cite this
MLA
Copy
Baranov, Pavel G., et al. “Synthesis and Structure of 1-Substituted Semithioglycolurils.” Synthesis, vol. 52, no. 17, May. 2020, pp. 2563-2571. https://doi.org/10.1055%2Fs-0040-1707391.