Synlett, volume 30, issue 3, pages 299-302
Direct Synthesis of 1-Alkyl-6-hydroxyalkyl-3a,6a-diphenylglycolurils from 1-Alkylimidazolinones and Their Cyclic Analogues
Publication type: Journal Article
Publication date: 2018-12-17
Organic Chemistry
Abstract
Two methods for the direct synthesis of previously inaccessible 1-alkyl-6-(hydroxyalkyl)-3a,6a-diphenylglycolurils have been developed as a result of a study of novel cyclocondensations of 1-alkylureas with tetrahydroimidazooxazolones, tetrahydroimidazooxazinones and 1-(hydroxyalkyl)ureas with 1-substituted imidazolinones. A mechanism to rationalize the highly regioselective formation of the target glycolurils is proposed.
Citations by journals
1
|
|
Synthesis
|
Synthesis
1 publication, 33.33%
|
Mendeleev Communications
|
Mendeleev Communications
1 publication, 33.33%
|
Russian Chemical Reviews
|
Russian Chemical Reviews
1 publication, 33.33%
|
1
|
Citations by publishers
1
|
|
Thieme
|
Thieme
1 publication, 33.33%
|
Elsevier
|
Elsevier
1 publication, 33.33%
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
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":[2020,2021],"ids":[0,0],"codes":[0,0],"imageUrls":["",""],"datasets":[{"label":"Citations number","data":[2,1],"backgroundColor":["#3B82F6","#3B82F6"],"percentage":["66.67","33.33"],"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":["Synthesis","Mendeleev Communications","Russian Chemical Reviews"],"ids":[10934,5294,23802],"codes":[0,0,0],"imageUrls":["\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_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":["Thieme","Elsevier","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii"],"ids":[135,17,9422],"codes":[0,0,0],"imageUrls":["\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_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 |
MLA
Cite this
GOST
Copy
Baranov P. G. et al. Direct Synthesis of 1-Alkyl-6-hydroxyalkyl-3a,6a-diphenylglycolurils from 1-Alkylimidazolinones and Their Cyclic Analogues // Synlett. 2018. Vol. 30. No. 3. pp. 299-302.
GOST all authors (up to 50)
Copy
Baranov P. G., Antonova M., Kolotyrkina N., Zanin I., Kravchenko A. Direct Synthesis of 1-Alkyl-6-hydroxyalkyl-3a,6a-diphenylglycolurils from 1-Alkylimidazolinones and Their Cyclic Analogues // Synlett. 2018. Vol. 30. No. 3. pp. 299-302.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1055/s-0037-1611937
UR - https://doi.org/10.1055%2Fs-0037-1611937
TI - Direct Synthesis of 1-Alkyl-6-hydroxyalkyl-3a,6a-diphenylglycolurils from 1-Alkylimidazolinones and Their Cyclic Analogues
T2 - Synlett
AU - Baranov, Pavel G.
AU - Antonova, Maria
AU - Kolotyrkina, Natalya
AU - Zanin, Igor
AU - Kravchenko, Angelina
PY - 2018
DA - 2018/12/17 00:00:00
PB - Thieme
SP - 299-302
IS - 3
VL - 30
SN - 0936-5214
SN - 1437-2096
ER -
Cite this
BibTex
Copy
@article{2018_Baranov,
author = {Pavel G. Baranov and Maria Antonova and Natalya Kolotyrkina and Igor Zanin and Angelina Kravchenko},
title = {Direct Synthesis of 1-Alkyl-6-hydroxyalkyl-3a,6a-diphenylglycolurils from 1-Alkylimidazolinones and Their Cyclic Analogues},
journal = {Synlett},
year = {2018},
volume = {30},
publisher = {Thieme},
month = {dec},
url = {https://doi.org/10.1055%2Fs-0037-1611937},
number = {3},
pages = {299--302},
doi = {10.1055/s-0037-1611937}
}
Cite this
MLA
Copy
Baranov, Pavel G., et al. “Direct Synthesis of 1-Alkyl-6-hydroxyalkyl-3a,6a-diphenylglycolurils from 1-Alkylimidazolinones and Their Cyclic Analogues.” Synlett, vol. 30, no. 3, Dec. 2018, pp. 299-302. https://doi.org/10.1055%2Fs-0037-1611937.