BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: De Nino A, Maiuolo L, Costanzo P, Algieri V, Jiritano A, Olivito F, Tallarida MA. Recent Progress in Catalytic Synthesis of 1,2,3-Triazoles. Catalysts 2021;11:1120. [DOI: 10.3390/catal11091120] [Cited by in Crossref: 8] [Cited by in F6Publishing: 10] [Article Influence: 4.0] [Reference Citation Analysis]
Number Citing Articles
1 Dey J, Yadav S, Raj Lakshkar R, Singh A, Ray S, Dash C. Zinc‐ bis (imino)pyridine Complexes as Catalysts for Azide‐Alkyne Cycloaddition in Water. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202202239] [Reference Citation Analysis]
2 Musalov MV, Potapov VA. Click Chemistry of Selenium Dihalides: Novel Bicyclic Organoselenium Compounds Based on Selenenylation/Bis-Functionalization Reactions and Evaluation of Glutathione Peroxidase-like Activity. Int J Mol Sci 2022;23. [PMID: 36555274 DOI: 10.3390/ijms232415629] [Reference Citation Analysis]
3 Algieri V, Costanzo P, Tallarida MA, Olivito F, Jiritano A, Fiorani G, Peccati F, Jiménez-Osés G, Maiuolo L, De Nino A. Regioselective Synthesis and Molecular Docking Studies of 1,5-Disubstituted 1,2,3-Triazole Derivatives of Pyrimidine Nucleobases. Molecules 2022;27. [PMID: 36500573 DOI: 10.3390/molecules27238467] [Reference Citation Analysis]
4 Al-Azmi A, John E. Construction of 5-(Alkylamino)-6-aryl/alkylpyrazine-2,3-dicarbonitriles via the One-Pot Reaction of Alkyl Isocyanides with Aryl/Alkyl Carbonyl Chlorides and Diaminomaleonitrile: Fluorescence and Antimicrobial Activity Evaluation. Molecules 2022;27. [PMID: 36500371 DOI: 10.3390/molecules27238278] [Reference Citation Analysis]
5 Božić B, Lađarević J, Petković M, Mijin D, Stavber S. Microwave Assisted Esterification of Aryl/Alkyl Acids Catalyzed by N-Fluorobenzenesulfonimide. Catalysts 2022;12:1413. [DOI: 10.3390/catal12111413] [Reference Citation Analysis]
6 Potapov VA, Musalov MV. Triple-Click Chemistry of Selenium Dihalides: Catalytic Regioselective and Highly Efficient Synthesis of Bis-1,2,3-Triazole Derivatives of 9-Selenabicyclo[3.3.1]nonane. Catalysts 2022;12:1032. [DOI: 10.3390/catal12091032] [Reference Citation Analysis]
7 Taniya OS, Fedotov VV, Novikov AS, Sadieva LK, Krinochkin AP, Kovalev IS, Kopchuk DS, Zyryanov GV, Liu Y, Ulomsky EN, Rusinov VL, Charushin VN. Abnormal push-pull benzo[4,5]imidazo[1,2-a][1,2,3]triazolo[4,5-e]pyrimidine fluorophores in planarized intramolecular charge transfer (PLICT) state: Synthesis, photophysical studies and theoretical calculations. Dyes and Pigments 2022;204:110405. [DOI: 10.1016/j.dyepig.2022.110405] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 De S, Aamna B, Sahu R, Parida S, Behera SK, Dan AK. Seeking heterocyclic scaffolds as antivirals against dengue virus. European Journal of Medicinal Chemistry 2022. [DOI: 10.1016/j.ejmech.2022.114576] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
9 Borah B, Chowhan LR. Ultrasound-assisted transition-metal-free catalysis: a sustainable route towards the synthesis of bioactive heterocycles. RSC Adv 2022;12:14022-51. [PMID: 35558846 DOI: 10.1039/d2ra02063g] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
10 Matin MM, Matin P, Rahman MR, Ben Hadda T, Almalki FA, Mahmud S, Ghoneim MM, Alruwaily M, Alshehri S. Triazoles and Their Derivatives: Chemistry, Synthesis, and Therapeutic Applications. Front Mol Biosci 2022;9:864286. [DOI: 10.3389/fmolb.2022.864286] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 10.0] [Reference Citation Analysis]
11 Schorr F, Arrowsmith M, Fantuzzi F, Rempel A, Braunschweig H. 1,2-Dialkynyldiboranes(4): B-B versus CC bond reactivity. Dalton Trans 2022;51:6197-203. [PMID: 35388860 DOI: 10.1039/d2dt00683a] [Reference Citation Analysis]
12 Niedballa J, Müller TJJ. Heterocycles by Consecutive Multicomponent Syntheses via Catalytically Generated Alkynoyl Intermediates. Catalysts 2022;12:90. [DOI: 10.3390/catal12010090] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]