Mendeleev Communications, volume 32, issue 2, pages 221-223

Diastereoselective cycloaddition of isatin azomethine ylides to 5-arylidene-2-thiohydantoins bearing 3-positioned chiral substituent

Barashkin Alexander A ¹

Shikut Nikita L ¹

Putilova Anastasia D ¹

Gorovoy Anton R ¹

Degtiarev Anton D ¹

Tafeenko Victor A.

Zyk Nikolai V. ¹

Tarasevich Boris N

Polyakov Vladislav S. ¹

Тафеенко В. А. ¹

Tarasevich B.N. ¹

Beloglazkina Elena K. ¹

Hide authors affiliations Show authors affiliations: 1 affiliation

Department of Chemistry, M. V. Lomonosov Moscow State University, 119991 Moscow, Russian Federation |

Publication type: Journal Article

Publication date: 2022-03-31

Elsevier

Journal: Mendeleev Communications

Quartile SCImago

Quartile WOS

Impact factor: 1.9

ISSN: 09599436, 1364551X

DOI: 10.1016/j.mencom.2022.03.022

Copy DOI

General Chemistry

Abstract

1,3-Dipolar cycloaddition of azomethine ylide, generated from isatin and sarcosine, with 5-arylidene-2-thiohydantoins equipped with various chiral substituents at the N 3 atom occurs diastereoselectively. The highest selectivity with dr = 5 : 1 was observed for the 2-thiohydantoin bearing 1,2-diphenylethyl substituent.

By date By citations

Citations by journals

	1 2
Mendeleev Communications	Mendeleev Communications, 2, 28.57% Mendeleev Communications 2 publications, 28.57%
Russian Journal of Organic Chemistry	Russian Journal of Organic Chemistry, 1, 14.29% Russian Journal of Organic Chemistry 1 publication, 14.29%
Advanced Synthesis and Catalysis	Advanced Synthesis and Catalysis, 1, 14.29% Advanced Synthesis and Catalysis 1 publication, 14.29%
New Journal of Chemistry	New Journal of Chemistry, 1, 14.29% New Journal of Chemistry 1 publication, 14.29%
Chemistry of Heterocyclic Compounds	Chemistry of Heterocyclic Compounds, 1, 14.29% Chemistry of Heterocyclic Compounds 1 publication, 14.29%
Russian Chemical Reviews	Russian Chemical Reviews, 1, 14.29% Russian Chemical Reviews 1 publication, 14.29%
	1 2

Citations by publishers

	1 2
Elsevier	Elsevier, 2, 28.57% Elsevier 2 publications, 28.57%
Pleiades Publishing	Pleiades Publishing, 1, 14.29% Pleiades Publishing 1 publication, 14.29%
Wiley	Wiley, 1, 14.29% Wiley 1 publication, 14.29%
Royal Society of Chemistry (RSC)	Royal Society of Chemistry (RSC), 1, 14.29% Royal Society of Chemistry (RSC) 1 publication, 14.29%
Springer Nature	Springer Nature, 1, 14.29% Springer Nature 1 publication, 14.29%
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii	Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii, 1, 14.29% Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii 1 publication, 14.29%
	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":[2022,2023],"ids":[0,0],"codes":[0,0],"imageUrls":["",""],"datasets":[{"label":"Citations number","data":[4,3],"backgroundColor":["#3B82F6","#3B82F6"],"percentage":["57.14","42.86"],"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","Russian Journal of Organic Chemistry","Advanced Synthesis and Catalysis","New Journal of Chemistry","Chemistry of Heterocyclic Compounds","Russian Chemical Reviews"],"ids":[5294,5728,3906,1404,16828,23802],"codes":[0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[2,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[28.57,14.29,14.29,14.29,14.29,14.29],"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","Pleiades Publishing","Wiley","Royal Society of Chemistry (RSC)","Springer Nature","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii"],"ids":[17,101,11,123,8,9422],"codes":[0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[2,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[28.57,14.29,14.29,14.29,14.29,14.29],"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 |

Cite this

GOST Copy

Barashkin A. A. et al. Diastereoselective cycloaddition of isatin azomethine ylides to 5-arylidene-2-thiohydantoins bearing 3-positioned chiral substituent // Mendeleev Communications. 2022. Vol. 32. No. 2. pp. 221-223.

GOST all authors (up to 50) Copy

Barashkin A. A., Shikut N. L., Putilova A. D., Gorovoy A. R., Degtiarev A. D., Tafeenko V. A., Tarasevich B. N., Zyk N. V., Polyakov V. S., Тафеенко В. А., Tarasevich B., Beloglazkina E. K. Diastereoselective cycloaddition of isatin azomethine ylides to 5-arylidene-2-thiohydantoins bearing 3-positioned chiral substituent // Mendeleev Communications. 2022. Vol. 32. No. 2. pp. 221-223.

RIS |

Cite this

RIS Copy

TY - JOUR

DO - 10.1016/j.mencom.2022.03.022

UR - https://doi.org/10.1016%2Fj.mencom.2022.03.022

TI - Diastereoselective cycloaddition of isatin azomethine ylides to 5-arylidene-2-thiohydantoins bearing 3-positioned chiral substituent

T2 - Mendeleev Communications

AU - Barashkin, Alexander A

AU - Shikut, Nikita L

AU - Putilova, Anastasia D

AU - Gorovoy, Anton R

AU - Degtiarev, Anton D

AU - Tafeenko, Victor A.

AU - Tarasevich, Boris N

AU - Zyk, Nikolai V.

AU - Polyakov, Vladislav S.

AU - Тафеенко, В. А.

AU - Tarasevich, B.N.

AU - Beloglazkina, Elena K.

PY - 2022

DA - 2022/03/31 00:00:00

PB - Elsevier

SP - 221-223

IS - 2

VL - 32

SN - 0959-9436

SN - 1364-551X

ER -

BibTex |

Cite this

BibTex Copy

@article{2022_Barashkin,

author = {Alexander A Barashkin and Nikita L Shikut and Anastasia D Putilova and Anton R Gorovoy and Anton D Degtiarev and Victor A. Tafeenko and Boris N Tarasevich and Nikolai V. Zyk and Vladislav S. Polyakov and В. А. Тафеенко and B.N. Tarasevich and Elena K. Beloglazkina},

title = {Diastereoselective cycloaddition of isatin azomethine ylides to 5-arylidene-2-thiohydantoins bearing 3-positioned chiral substituent},

journal = {Mendeleev Communications},

year = {2022},

volume = {32},

publisher = {Elsevier},

month = {mar},

url = {https://doi.org/10.1016%2Fj.mencom.2022.03.022},

number = {2},

pages = {221--223},

doi = {10.1016/j.mencom.2022.03.022}

}

MLA

Cite this

MLA Copy

Barashkin, Alexander A., et al. “Diastereoselective cycloaddition of isatin azomethine ylides to 5-arylidene-2-thiohydantoins bearing 3-positioned chiral substituent.” Mendeleev Communications, vol. 32, no. 2, Mar. 2022, pp. 221-223. https://doi.org/10.1016%2Fj.mencom.2022.03.022.

Found error?

Publisher

Elsevier

Journal

Mendeleev Communications

Quartile SCImago

Quartile WOS

Impact factor

1.9

ISSN

09599436 (Print)
1364551X (Electronic)

Labs

Laboratory of Biologically Active Organic Compounds (BAOС)

Profiles

Beloglazkina, Elena K