Scopus by Title (Ref)
Articles that cite the referenced work, matched by title from the Scopus database.
An Active Group with Potential Anti-seizure Activity: A Review on 1,2,4- Triazoles
Letters in Drug Design and Discovery
2023
Wang Y.
Synthesis, Antifungal, and Antioxidant Evaluation of New Class of Thiazoloquinazoline Linked by Carbonyl with Nitrile, Phenylacrylonitrile, Pyrazole, Pyrazolo[1,5-a]pyrimidine and Triazolo[1,5-a]pyrimidine as Five and Six-Membered Heterocycles Derivatives
Russian Journal of Bioorganic Chemistry
December 2022
Saleh E.A.M.
An Overview on Synthetic and Medicinal Perspectives of [1,2,4]Triazolo[1,5-a]pyrimidine Scaffold
Chemistry and Biodiversity
September 2022
Merugu S.R.
An Important Potential Anti-Epileptic/Anticonvulsant Active Group: A Review of 1,2,4-Triazole Groups and Their Action
Drug Research
1 March 2021
Wang Y.
Biological activities of [1,2,4]triazolo[1,5-a]pyrimidines and analogs
Medicinal Chemistry Research
1 October 2020
Pinheiro S.
DABCO-catalyzed Five-component Domino Protocol for the Synthesis of Novel Benzo[a]pyrazolo[4’,3’:5,6]pyrano[2,3-c]phenazines in PEG-400 as an Efficient Green Reaction Medium
Organic Preparations and Procedures International
3 July 2020
Yazdani-Elah-Abadi A.
Microwave-assisted Multi-component Domino Reaction for the Green Synthesis of Novel Benzo[a]pyrano[3',4':5,6]pyrano[2,3-c]phenazines Using H3PW12O40 as Efficient, Cost-effective and Recyclable Catalyst
Organic Preparations and Procedures International
3 September 2019
Mohammadrezaei M.
Recent advances in 1,2,4-triazolo[1,5-a]pyrimidine chemistry
Advances in Heterocyclic Chemistry
1 January 2019
Fischer G.
H3PW12O40@nano-ZnO: An efficient, recyclable, and eco-friendly catalyst for the green synthesis of novel benzo[a]pyrimido[5′,4′:5,6]pyrano[2,3-c]phenazines via sequential multicomponent reactions under microwave irradiation
Journal of the Chinese Chemical Society
August 2018
Mohammadrezaei M.
Novel Multicomponent Synthesis of Pyridine-Pyrimidines and Their Bis-Derivatives Catalyzed by Triazine Diphosphonium Hydrogen Sulfate Ionic Liquid Supported on Functionalized Nanosilica
ACS Combinatorial Science
8 January 2018
Rahmani F.
Recent developments on triazole nucleus in anticonvulsant compounds: a review
Journal of Enzyme Inhibition and Medicinal Chemistry
1 January 2018
Song M.X.
Open Access
Synthesis and neurotropic activity of the derivatives of fused triazolo[4,3-c]- and triazolo[1,5-c]pyrimidines
Russian Journal of Bioorganic Chemistry
1 September 2017
Paronikyan E.
Media and solute–solvent interaction effects on the photo–physical behavior of some drugs of 4H–Pyran derivatives
Journal of Molecular Liquids
1 July 2017
Kian R.
3,4-DHQLO and triazole and its related analogues with anticonvulsant effects
Mini Reviews in Medicinal Chemistry
1 March 2016
Guan L.
The importance of triazole scaffold in the development of anticonvulsant agents
European Journal of Medicinal Chemistry
15 February 2016
Ayati A.
Synthesis and anticonvulsant activity evaluation of 3-alkoxy-4-(4-(hexyloxy/heptyloxy)phenyl)-4h-1,2,4 -triazole
Iranian Journal of Pharmaceutical Research
1 December 2015
Fang Y.Q.
Synthesis and neurotropic activity of 2,4-disubstituted pyrano[4',3':4,5]pyrido[2,3-b]thieno[3,2-d]pyrimidines
Russian Journal of Bioorganic Chemistry
November 2015
Paronikyan E.
Synthesis and antimicrobial activity of some tetrahydro quinolone diones and pyrano[2,3-d]pyrimidine derivatives
Iranian Journal of Pharmaceutical Research
1 March 2015
Shahi M.
1,2,4-triazole derivatives as potential scaffold for anticonvulsant activity
Central Nervous System Agents in Medicinal Chemistry
2015
Kamboj V.
Pyrimidine derivatives as potential agents acting on central nervous system
Central Nervous System Agents in Medicinal Chemistry
2015
Kumar S.
Synthesis of some novel chromenopyrimidine derivatives and evaluation of their biological activities
Iranian Journal of Pharmaceutical Research
2014
Mobinikhaledi A.
Synthesis and antiseizure evaluation of isoindoline-1,3-dione derivatives in mice
Medicinal Chemistry Research
June 2014
Aliabadi A.