Chemistry of Heterocyclic Compounds, volume 50, issue 11, pages 1515-1527
Oxoindolinylidene Derivatives of Thiazolidin-4-ones: Methods of Synthesis and Biological Activity (Review)
Gazieva G A
1
,
Izmestev A N
1
Publication type: Journal Article
Publication date: 2015-01-06
Journal:
Chemistry of Heterocyclic Compounds
Quartile SCImago
Q3
Quartile WOS
Q3
Impact factor: 1.5
ISSN: 00093122, 15738353
Organic Chemistry
Abstract
We offer a review on synthetic methods and biological activity data for oxoindolinylidene derivatives of thiazolidin-4-ones, including heteroannelated examples of such compounds, published between 1967 and 2014.
Citations by journals
|
1
2
3
|
|
|
Research on Chemical Intermediates
|
Research on Chemical Intermediates
3 publications, 15.79%
|
|
New Journal of Chemistry
|
New Journal of Chemistry
2 publications, 10.53%
|
|
Molecules
|
Molecules
2 publications, 10.53%
|
|
Chemistry of Heterocyclic Compounds
|
Chemistry of Heterocyclic Compounds
2 publications, 10.53%
|
|
RSC Advances
|
RSC Advances
1 publication, 5.26%
|
|
Beilstein Journal of Organic Chemistry
|
Beilstein Journal of Organic Chemistry
1 publication, 5.26%
|
|
ChemistrySelect
|
ChemistrySelect
1 publication, 5.26%
|
|
Mendeleev Communications
|
Mendeleev Communications
1 publication, 5.26%
|
|
Journal of Organometallic Chemistry
|
Journal of Organometallic Chemistry
1 publication, 5.26%
|
|
European Journal of Medicinal Chemistry
|
European Journal of Medicinal Chemistry
1 publication, 5.26%
|
|
ChemInform
|
ChemInform
1 publication, 5.26%
|
|
Journal of Heterocyclic Chemistry
|
Journal of Heterocyclic Chemistry
1 publication, 5.26%
|
|
Journal of Organic Chemistry
|
Journal of Organic Chemistry
1 publication, 5.26%
|
|
Organic and Biomolecular Chemistry
|
Organic and Biomolecular Chemistry
1 publication, 5.26%
|
|
1
2
3
|
Citations by publishers
|
1
2
3
4
5
|
|
|
Springer Nature
|
Springer Nature
5 publications, 26.32%
|
|
Royal Society of Chemistry (RSC)
|
Royal Society of Chemistry (RSC)
4 publications, 21.05%
|
|
Wiley
|
Wiley
3 publications, 15.79%
|
|
Elsevier
|
Elsevier
3 publications, 15.79%
|
|
Multidisciplinary Digital Publishing Institute (MDPI)
|
Multidisciplinary Digital Publishing Institute (MDPI)
2 publications, 10.53%
|
|
Beilstein-Institut
|
Beilstein-Institut
1 publication, 5.26%
|
|
American Chemical Society (ACS)
|
American Chemical Society (ACS)
1 publication, 5.26%
|
|
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":[2015,2016,2017,2018,2019,2020,2021,2022,2023],"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":[2,1,4,1,3,1,1,3,3],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["10.53","5.26","21.05","5.26","15.79","5.26","5.26","15.79","15.79"],"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":["Research on Chemical Intermediates","New Journal of Chemistry","Molecules","Chemistry of Heterocyclic Compounds","RSC Advances","Beilstein Journal of Organic Chemistry","ChemistrySelect","Mendeleev Communications","Journal of Organometallic Chemistry","European Journal of Medicinal Chemistry","ChemInform","Journal of Heterocyclic Chemistry","Journal of Organic Chemistry","Organic and Biomolecular Chemistry"],"ids":[10787,1404,1770,16828,3100,21928,8021,5294,11834,8171,25372,3189,8697,541],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp"],"datasets":[{"label":"","data":[3,2,2,2,1,1,1,1,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[15.79,10.53,10.53,10.53,5.26,5.26,5.26,5.26,5.26,5.26,5.26,5.26,5.26,5.26],"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","Royal Society of Chemistry (RSC)","Wiley","Elsevier","Multidisciplinary Digital Publishing Institute (MDPI)","Beilstein-Institut","American Chemical Society (ACS)"],"ids":[8,123,11,17,202,6139,40],"codes":[0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp"],"datasets":[{"label":"","data":[5,4,3,3,2,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[26.32,21.05,15.79,15.79,10.53,5.26,5.26],"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., Izmestev A. N. Oxoindolinylidene Derivatives of Thiazolidin-4-ones: Methods of Synthesis and Biological Activity (Review) // Chemistry of Heterocyclic Compounds. 2015. Vol. 50. No. 11. pp. 1515-1527.
GOST all authors (up to 50)
Copy
Gazieva G. A., Izmestev A. N. Oxoindolinylidene Derivatives of Thiazolidin-4-ones: Methods of Synthesis and Biological Activity (Review) // Chemistry of Heterocyclic Compounds. 2015. Vol. 50. No. 11. pp. 1515-1527.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1007/S10593-014-1619-8
UR - https://doi.org/10.1007%2FS10593-014-1619-8
TI - Oxoindolinylidene Derivatives of Thiazolidin-4-ones: Methods of Synthesis and Biological Activity (Review)
T2 - Chemistry of Heterocyclic Compounds
AU - Gazieva, G A
AU - Izmestev, A N
PY - 2015
DA - 2015/01/06 00:00:00
PB - Springer Nature
SP - 1515-1527
IS - 11
VL - 50
SN - 0009-3122
SN - 1573-8353
ER -
Cite this
BibTex
Copy
@article{2015_Gazieva,
author = {G A Gazieva and A N Izmestev},
title = {Oxoindolinylidene Derivatives of Thiazolidin-4-ones: Methods of Synthesis and Biological Activity (Review)},
journal = {Chemistry of Heterocyclic Compounds},
year = {2015},
volume = {50},
publisher = {Springer Nature},
month = {jan},
url = {https://doi.org/10.1007%2FS10593-014-1619-8},
number = {11},
pages = {1515--1527},
doi = {10.1007/S10593-014-1619-8}
}
Cite this
MLA
Copy
Gazieva, G. A., and A N Izmestev. “Oxoindolinylidene Derivatives of Thiazolidin-4-ones: Methods of Synthesis and Biological Activity (Review).” Chemistry of Heterocyclic Compounds, vol. 50, no. 11, Jan. 2015, pp. 1515-1527. https://doi.org/10.1007%2FS10593-014-1619-8.
Profiles