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Cited by in F6Publishing
For: Baykov S, Semenov A, Tarasenko M, Boyarskiy VP. Application of amidoximes for the heterocycles synthesis. Tetrahedron Letters 2020;61:152403. [DOI: 10.1016/j.tetlet.2020.152403] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 3.3] [Reference Citation Analysis]
Number Citing Articles
1 Presnukhina SI, Tarasenko MV, Geyl KK, Baykova SO, Baykov SV, Shetnev AA, Boyarskiy VP. Unusual Formation of 1,2,4-Oxadiazine Core in Reaction of Amidoximes with Maleic or Fumaric Esters. Molecules 2022;27:7508. [DOI: 10.3390/molecules27217508] [Reference Citation Analysis]
2 Baykov S, Tarasenko M, Kotlyarova V, Shetnev A, Zelenkov LE, Boyarskaya IA, Boyarskiy VP. 2‐(1,2,4‐Oxadiazol‐5‐yl)aniline as a New Scaffold for Blue Luminescent Materials. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202201201] [Reference Citation Analysis]
3 Baykov SV, Tarasenko MV, Semenov AV, Katlenok EA, Shetnev AA, Boyarskiy VP. Dualism of 1,2,4-oxadiazole ring in noncovalent interactions with carboxylic group. Journal of Molecular Structure 2022;1262:132974. [DOI: 10.1016/j.molstruc.2022.132974] [Reference Citation Analysis]
4 Sidneva VV, Tarasenko MV, Kofanov ER. One-pot synthesis of 3,5-disubstituted 1,2,4-oxadiazoles containing an alkenyl moiety. Chem Heterocycl Comp. [DOI: 10.1007/s10593-022-03096-5] [Reference Citation Analysis]
5 Os’kina IA, Vinogradov AS, Selivanov BA, Savelyev VA, Platonov VE, Tikhonov AY. Synthesis of 4,5-Dialkyl-2-perfluoroaryl-1H-imidazol-1-ols and 4,5-Dimethyl-2-perfluoroaryl-1H-imidazoles. Russ J Org Chem 2021;57:1968-73. [DOI: 10.1134/s1070428021120101] [Reference Citation Analysis]
6 Hlubb LN, Johnson EC, Sabatini JJ, Orlicki JA. Scalable and Safe Transformation of 3-Hydroxypropionitrile to Its Amidoxime. Org Process Res Dev 2022;26:195-8. [DOI: 10.1021/acs.oprd.1c00401] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Belen’kii LI, Gazieva GA, Evdokimenkova YB, Soboleva NO. The literature of heterocyclic chemistry, Part XX, 2020. Advances in Heterocyclic Chemistry 2022. [DOI: 10.1016/bs.aihch.2022.10.005] [Reference Citation Analysis]
8 Tarasenko MV, Kotlyarova VD, Baykov SV, Shetnev AA. 2-(1,2,4-Oxadiazol-5-yl)anilines Based on Amidoximes and Isatoic Anhydrides: Synthesis and Structure Features. Russ J Gen Chem 2021;91:768-78. [DOI: 10.1134/s1070363221050030] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
9 Tret’yakova EV. Synthesis of Tetrazole and 1,2,4-Oxadiazole Derivatives of Maleopimaric Acid Methyl Ester. Russ J Org Chem 2021;57:391-5. [DOI: 10.1134/s1070428021030106] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
10 Yet L. Five-membered ring systems: with more than one N atom. Progress in Heterocyclic Chemistry 2021. [DOI: 10.1016/b978-0-323-98410-2.00008-4] [Reference Citation Analysis]
11 Zhang L, Su J, Xu X. Design and Synthesis of 1,2,4-Oxadiazine Derivatives as Promising Fungicide and Insecticide Lead Compound. Chinese Journal of Organic Chemistry 2021;41:3539. [DOI: 10.6023/cjoc202101029] [Reference Citation Analysis]