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Cited by in F6Publishing
For: Zribi L, Zribi F, Marco-contelles J, Chabchoub F, Ismaili L. Facile one-pot synthesis of new [1,2,4]triazolo[1,5- a ]pyridine derivatives by ultrasonic irradiation. Synthetic Communications 2017;47:1934-9. [DOI: 10.1080/00397911.2017.1357078] [Cited by in Crossref: 9] [Cited by in F6Publishing: 1] [Article Influence: 1.8] [Reference Citation Analysis]
Number Citing Articles
1 Keerthy HK, Mohan S, Basappa, Bharathkumar H, Rangappa S, Svensson F, Bender A, Mohan CD, Rangappa KS, Bhatnagar R. Triazole-Pyridine Dicarbonitrile Targets Phosphodiesterase 4 to Induce Cytotoxicity in Lung Carcinoma Cells. Chem Biodivers 2019;16:e1900234. [PMID: 31287204 DOI: 10.1002/cbdv.201900234] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 1.7] [Reference Citation Analysis]
2 Vorob’ev AY. Methods of synthesis of [1,2,4]triazolo[1,5-а]pyridines (microreview). Chem Heterocycl Comp 2019;55:695-7. [DOI: 10.1007/s10593-019-02522-5] [Cited by in Crossref: 3] [Article Influence: 1.0] [Reference Citation Analysis]
3 Khomenko DM, Shokol TV, Doroshchuk RO, Starova VS, Raspertova IV, Shova S, Lampeka RD, Volovenko YM. An alternative approach to the synthesis of [1,2,4]triazolo[1,5‐ a ]pyridine‐8‐carbonitriles, their crystal structure, and DFT calculations. J Heterocyclic Chem 2021;58:1278-85. [DOI: 10.1002/jhet.4256] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]