Аннотация:
Organic compounds bearing semi-polar nitrogen–oxygen bonds are considered as perspective platform for designing socially important medications and high energy materials. Herein, recently developed original syntheses of monocyclic and fused 1,2,3,4-tetrazine 1,3-dioxides, various (methylene)bis(1-oxy-1-triazene 2-oxide) derivatives, furoxan-containing polyheterocyclic scaffolds and diastereoor enantiomerically enriched functionalized aliphatic nitro compounds are summarized. Prospects for their practical applications are outlined.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
S. G. Zlotin, A. M. Churakov, O. A. Luk'yanov, N. N. Makhova, A. Yu. Sukhorukov, V. A. Tartakovsky, “Novel approaches to pharmacology-oriented and energy rich organic nitrogen–oxygen systems”, Mendeleev Commun., 25:6 (2015), 399–409
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc2425
https://www.mathnet.ru/rus/mendc/v25/i6/p399
Эта публикация цитируется в следующих 65 статьяx:
G. V. Pokhvisneva, S. D. Budina, G. A. Smirnov, “Reaction of arylsulfonyl chlorides with 1-methoxy-3-methyltriaz-1-ene 2-oxide sodium salt”, Russ Chem Bull, 73:5 (2024), 1328
Tijana Lj. Šestić, Jovana J. Ajduković, Maja A. Marinović, Edward T. Petri, Marina P. Savić, “In silico ADMET analysis of the A-, B- and D-modified androstane derivatives with potential anticancer effects”, Steroids, 189 (2023), 109147
P. B. Gordeev, G. A. Smirnov, “Alkylation of oxytriazene oxide salts with 2-(chloromethoxy)diazene 1-oxide derivatives”, Russ Chem Bull, 72:7 (2023), 1584
Oznur Eyilcim, Fulya Gunay, Omer Tahir Gunkara, Yuk Yin Ng, Ozlem Ulucan, Ihsan Erden, “Design and synthesis of novel 1,2,3,4‐tetrazines as new anti‐leukemia cancer agents”, Chem Biol Drug Des, 102:5 (2023), 1186
A. A. Konnov, M. S. Klenov, A. M. Churakov, Yu. A. Strelenko, K. A. Lyssenko, V. A. Tartakovsky, “Synthesis and crystal structure of the first amino-1,3a,4,6a-tetraazapentalenes”, Mendeleev Commun., 30:2 (2020), 139–141
С. Г. Злотин, И. Л. Далингер, Н. Н. Махова, В. А. Тартаковский, “Нитросоединения — структурная основа перспективных энергоемких материалов и многоцелевые реагенты для органического синтеза”, Усп. хим., 89:1 (2020), 1–54; S. G. Zlotin, I. L. Dalinger, N. N. Makhova, V. A. Tartakovsky, “Nitro compounds as the core structures of promising energetic materials and versatile reagents for organic synthesis”, Russian Chem. Reviews, 89:1 (2020), 1–54
A. A. Konnov, M. S. Klenov, A. M. Churakov, Yu. A. Strelenko, I. V. Fedyanin, V. A. Tartakovsky, “An unusual reduction of azido group accompanied by ring closure to 1,2,3-triazole 3-oxide”, Russ Chem Bull, 68:1 (2019), 191
G. A. Smirnov, P. B. Gordeev, S. V. Nikitin, G. V. Pokhvisneva, T. V. Ternikova, I. M. Chistokhvalov, O. A. Luk'yanov, “N-(2-Azidoethyl) derivatives of methylenebis(1-oxytriaz-1-ene 2-oxides)”, Russ Chem Bull, 67:11 (2018), 2010
L. S. Konstantinova, E. A. Knyazeva, Yu. V. Gatilov, S. G. Zlotin, O. A. Rakitin, “Nitro derivatives of 2,1,3-benzothiadiazole 1-oxides: synthesis, structural study, and NO release”, Russ Chem Bull, 67:1 (2018), 95
D. B. Lempert, A. I. Kazakov, S. I. Soglasnova, I. L. Dalinger, A. B. Sheremetev, “Energetic abilities of nitro derivatives of isomeric (pyrazol-3-yl)tetrazoles as components of solid composite propellants”, Russ Chem Bull, 67:9 (2018), 1580
Anatoly N. Vereshchagin, Michail N. Elinson, Yuliya E. Anisina, Kirill A. Karpenko, Alexander S. Goloveshkin, Sergey G. Zlotin, Mikhail P. Egorov, “High diastereoselective amine-catalyzed Knoevenagel–Michael-cyclization–ring-opening cascade between aldehydes, 3-arylisoxazol-5(4H)-ones and 3-aminocyclohex-2-en-1-ones”, Mol Divers, 22:3 (2018), 627
P. B. Gordeev, G. A. Smirnov, S. V. Nikitin, G. V. Pokhvisneva, T. V. Ternikova, O. A. Luk'yanov, “Synthesis of N-β-haloethyl derivatives of bis(oxytriazene oxides) bearing the NCH2O fragment”, Russ Chem Bull, 67:1 (2018), 85
G. V. Pokhvisneva, P. B. Gordeev, S. V. Nikitin, G. A. Smirnov, T. V. Ternikova, O. A. Luk'yanov, “3,3-Bis(2-nitroxyethyl) derivatives of 1,1′-[methylenebis(oxy)]bis(triaz-1-ene 2-oxides) as a new type of NO donors”, Russ Chem Bull, 67:9 (2018), 1655
S. V. Nikitin, G. V. Pokhvisneva, T. V. Ternikova, P. B. Gordeev, I. M. Chistokhvalov, G. A. Smirnov, O. A. Luk'yanov, “N-β-Nitroxyethyl derivatives of 1,1'-[methylenebis(oxy)]bis(triaz-1-ene 2-oxides)”, Russ Chem Bull, 67:8 (2018), 1445
G. A. Smirnov, P. B. Gordeev, S. V. Nikitin, G. V. Pokhvisneva, T. V. Ternikova, I. M. Chistokhvalov, O. A. Luk'yanov, “Bis-, tris-, and tetrakis-N-(2-nitroxyethyl) derivatives of 1,1'-[methylenebis(oxy)]bis(triaz-1-ene 2-oxides)”, Russ Chem Bull, 67:9 (2018), 1662
Alexey M. Starosotnikov, Maxim A. Bastrakov, Vadim V. Kachala, Ivan V. Fedyanin, Svyatoslav A. Shevelev, Igor L. Dalinger, “Unusual Pericyclic Reactivity of 4‐Nitrobenzofuroxans in 1,3‐Dipolar Cycloaddition with N‐Benzyl Azomethine Ylide – A New Example of Multiple C–C‐Bond Forming Transformations.”, ChemistrySelect, 3:34 (2018), 9773
Nina N. Makhova, Oleg A. Rakitin, “Furoxans fused with heterocycles as promising donors and precursors for nitric oxide donors (microreview)”, Chem Heterocycl Comp, 53:8 (2017), 849
Alexander A. Larin, Leonid L. Fershtat, Ivan V. Ananyev, Nina N. Makhova, “Versatile approach to heteroarylfuroxan derivatives from oximinofuroxans via a one-pot, nitration/thermolysis/[3+2]-cycloaddition cascade”, Tetrahedron Letters, 58:42 (2017), 3993
Vladimir A. Motornov, Andrey A. Tabolin, Roman A. Novikov, Yulia V. Nelyubina, Sema L. Ioffe, Ivan V. Smolyar, Valentine G. Nenajdenko, “Synthesis and Regioselective N‐2 Functionalization of 4‐Fluoro‐5‐aryl‐1,2,3‐NH‐triazoles”, Eur J Org Chem, 2017:46 (2017), 6851
Alexey M Starosotnikov, Dmitry V Shkaev, Maxim A Bastrakov, Ivan V Fedyanin, Svyatoslav A Shevelev, Igor L Dalinger, “Nucleophilic dearomatization of 4-aza-6-nitrobenzofuroxan by CH acids in the synthesis of pharmacology-oriented compounds”, Beilstein J. Org. Chem., 13 (2017), 2854
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