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For: Malki Y, Martinez J, Masurier N. 1,3-Diazepine: A privileged scaffold in medicinal chemistry. Med Res Rev 2021;41:2247-315. [PMID: 33645848 DOI: 10.1002/med.21795] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
Number Citing Articles
1 Belal A, Abdel Gawad NM, Mehany ABM, Abourehab MAS, Elkady H, Al-Karmalawy AA, Ismael AS. Design, synthesis and molecular docking of new fused 1H-pyrroles, pyrrolo[3,2-d]pyrimidines and pyrrolo[3,2-e][1, 4]diazepine derivatives as potent EGFR/CDK2 inhibitors. J Enzyme Inhib Med Chem 2022;37:1884-902. [PMID: 35801486 DOI: 10.1080/14756366.2022.2096019] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 6.0] [Reference Citation Analysis]
2 Nasiriani T, Javanbakht S, Nazeri MT, Farhid H, Khodkari V, Shaabani A. Isocyanide-Based Multicomponent Reactions in Water: Advanced Green Tools for the Synthesis of Heterocyclic Compounds. Top Curr Chem (Cham) 2022;380:50. [PMID: 36136281 DOI: 10.1007/s41061-022-00403-8] [Reference Citation Analysis]
3 Zhang H, Liu R, Lou T, Zhao P, Wang S. Pentostatin Biosynthesis Pathway Elucidation and Its Application. Fermentation 2022;8:459. [DOI: 10.3390/fermentation8090459] [Reference Citation Analysis]
4 Malki Y, Maillard LT, Masurier N. 1,3‐Diazepine Derivatives: Strategies for Synthesis. Eur J Org Chem 2022;2022. [DOI: 10.1002/ejoc.202100492] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]