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For: Makhova NN, Fershtat LL. Recent advances in the synthesis and functionalization of 1,2,5-oxadiazole 2-oxides. Tetrahedron Letters 2018;59:2317-26. [DOI: 10.1016/j.tetlet.2018.04.070] [Cited by in Crossref: 24] [Cited by in F6Publishing: 12] [Article Influence: 6.0] [Reference Citation Analysis]
Number Citing Articles
1 Zhang Q, Zhao C, Zhang X, He C, Pang S. Oxidation of o -dioxime by (diacetoxyiodo)benzene: green and mild access to furoxans. New J Chem 2022;46:1489-93. [DOI: 10.1039/d1nj05510k] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
2 Bystrov DM, Zhilin ES, Fershtat LL, Romanova AA, Ananyev IV, Makhova NN. Tandem Condensation/Rearrangement Reaction of 2-Aminohetarene N -Oxides for the Synthesis of Hetaryl Carbamates. Adv Synth Catal 2018;360:3157-63. [DOI: 10.1002/adsc.201800407] [Cited by in Crossref: 13] [Cited by in F6Publishing: 6] [Article Influence: 3.3] [Reference Citation Analysis]
3 Belyakov A, Oskorbin A, Losev V, Rykov A, Shishkov I, Fershtat L, Larin A, Kuznetsov V, Makhova N. The equilibrium molecular structure of 3-methyl-4-nitro- and 4-methyl-3-nitrofuroxans by gas-phase electron diffraction and coupled cluster calculations. Journal of Molecular Structure 2020;1222:128856. [DOI: 10.1016/j.molstruc.2020.128856] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
4 Fershtat LL, Teslenko FE. Five-Membered Hetarene N-Oxides: Recent Advances in Synthesis and Reactivity. Synthesis 2021;53:3673-82. [DOI: 10.1055/a-1529-7678] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Pukhov SA, Anikina LA, Larin AA, Fershtat LL, Kulikov AS, Makhova NN. Hetarylfuroxans: cytotoxic effect and induction of apoptosis in chronic myeloid leukemia K562 cells. Russ Chem Bull 2019;68:158-62. [DOI: 10.1007/s11172-019-2431-5] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
6 Zhilin ES, Bystrov DM, Ananyev IV, Fershtat LL, Makhova NN. Straightforward Access to the Nitric Oxide Donor Azasydnone Scaffold by Cascade Reactions of Amines. Chem Eur J 2019;25:14284-9. [DOI: 10.1002/chem.201903526] [Cited by in Crossref: 11] [Cited by in F6Publishing: 5] [Article Influence: 3.7] [Reference Citation Analysis]
7 Zhilin ES, Fershtat LL, Bystrov DM, Kulikov AS, Dmitrienko AO, Ananyev IV, Makhova NN. Renaissance of 1,2,5-Oxadiazolyl Diazonium Salts: Synthesis and Reactivity: Renaissance of 1,2,5-Oxadiazolyl Diazonium Salts: Synthesis and Reactivity. Eur J Org Chem 2019;2019:4248-59. [DOI: 10.1002/ejoc.201900622] [Cited by in Crossref: 9] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
8 Poonam, Bhasin G, Srivastava R, Singh R. Oxadiazoles: moiety to synthesis and utilize. J IRAN CHEM SOC 2022;19:665-77. [DOI: 10.1007/s13738-021-02335-4] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Bystrov DM, Ananyev IV, Fershtat LL, Makhova NN. Direct Synthesis of N-(1,2,5-Oxadiazolyl)hydrazones through a Diazotization/Reduction/Condensation Cascade. J Org Chem 2020;85:15466-75. [PMID: 33185453 DOI: 10.1021/acs.joc.0c02243] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
10 Fershtat LL, Makhova NN. 1,2,5‐Oxadiazole‐Based High‐Energy‐Density Materials: Synthesis and Performance. ChemPlusChem 2020;85:13-42. [DOI: 10.1002/cplu.201900542] [Cited by in Crossref: 43] [Cited by in F6Publishing: 9] [Article Influence: 14.3] [Reference Citation Analysis]
11 Luk′yanov OA, Parakhin VV, Shlykova NI, Dmitrienko AO, Melnikova EK, Kon'kova TS, Monogarov KA, Meerov DB. Energetic N -azidomethyl derivatives of polynitro hexaazaisowurtzitanes series: CL-20 analogues having the highest enthalpy. New J Chem 2020;44:8357-65. [DOI: 10.1039/d0nj01453b] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 2.5] [Reference Citation Analysis]
12 Plumet J. 1,3-Dipolar Cycloaddition Reactions of Nitrile Oxides under "Non-Conventional" Conditions: Green Solvents, Irradiation, and Continuous Flow. Chempluschem 2020;85:2252-71. [PMID: 33044044 DOI: 10.1002/cplu.202000448] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 5.0] [Reference Citation Analysis]
13 Gu Z, Guo F, Zhang P, Qin Y, Guo Z. Solvent-free mechanochemical synthesis of diacylfuroxans. Tetrahedron Letters 2019;60:1687-90. [DOI: 10.1016/j.tetlet.2019.05.024] [Cited by in Crossref: 6] [Article Influence: 2.0] [Reference Citation Analysis]
14 Kulikov AS, Epishina MA, Churakov AI, Anikina LV, Fershtat LL, Makhova NN. Regioselective synthesis, structural diversification and cytotoxic activity of (thiazol-4-yl)furoxans. Mendeleev Communications 2018;28:623-5. [DOI: 10.1016/j.mencom.2018.11.020] [Cited by in Crossref: 8] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
15 Zhang R, Xu X, Ma P, Ma C, Zhai D, Pan Y, Jiang J. High-energy materials based on 1H-tetrazole and furoxan: Molecular design and screening. Journal of Molecular Structure 2022;1250:131900. [DOI: 10.1016/j.molstruc.2021.131900] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
16 Teslenko FE, Churakov AI, Larin AA, Ananyev IV, Fershtat LL, Makhova NN. Route to 1,2,4- and 1,2,5-oxadiazole ring assemblies via a one-pot condensation/oxidation protocol. Tetrahedron Letters 2020;61:151678. [DOI: 10.1016/j.tetlet.2020.151678] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
17 Liu Z, Liu Q, Zhang B, Liu Q, Fang L, Gou S. Blood-Brain Barrier Permeable and NO-Releasing Multifunctional Nanoparticles for Alzheimer's Disease Treatment: Targeting NO/cGMP/CREB Signaling Pathways. J Med Chem 2021;64:13853-72. [PMID: 34517696 DOI: 10.1021/acs.jmedchem.1c01240] [Reference Citation Analysis]
18 Kukuljan L, Kranjc K. 3-(5-Amino-1,2,4-triazole)-1,2,4-oxadiazole: A new biheterocyclic scaffold for the synthesis of energetic materials. Tetrahedron Letters 2019;60:207-9. [DOI: 10.1016/j.tetlet.2018.12.014] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
19 Epishina MA, Kulikov AS, Fershtat LL, Ananyev IV, Makhova NN. Synthesis of new pharmacologically oriented heterocyclic ensembles, [2-(1H-pyrazol-1-yl)thiazol-4-yl]furoxans. Mendeleev Communications 2019;29:288-91. [DOI: 10.1016/j.mencom.2019.05.015] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
20 Larin AA, Muravyev NV, Pivkina AN, Suponitsky KY, Ananyev IV, Khakimov DV, Fershtat LL, Makhova NN. Assembly of Tetrazolylfuroxan Organic Salts: Multipurpose Green Energetic Materials with High Enthalpies of Formation and Excellent Detonation Performance. Chem Eur J 2019;25:4225-33. [DOI: 10.1002/chem.201806378] [Cited by in Crossref: 30] [Cited by in F6Publishing: 13] [Article Influence: 10.0] [Reference Citation Analysis]
21 Kulikov AS, Epishina MA, Zhilin ES, Shuvaev AD, Fershtat LL, Makhova NN. Design and synthesis of pyrazolo[3,4-d]pyridazine 5,6-dioxides as novel NO-donors. Mendeleev Communications 2021;31:42-5. [DOI: 10.1016/j.mencom.2021.01.012] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
22 Fouad FS, Ness T, Wang K, Ruth CE, Britton S, Twieg RJ. Biphenylyl-1,2,4-oxadiazole based liquid crystals – synthesis, mesomorphism, effect of lateral monofluorination. Liquid Crystals 2019;46:2281-90. [DOI: 10.1080/02678292.2019.1623335] [Cited by in Crossref: 9] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]