Аннотация:
SnCl4-promoted [4 + 2] cycloaddition of β-nitrostyrenes to 4-methylidene-1,3-dioxolane provides stereoselective synthesis of spirocyclic nitronates. 2-Nitrovinyl benzoate under the same conditions produces δ-substituted nitrodiene as a single E,E-isomer.
Образец цитирования:
A. A. Mikhaylov, P. A. Zhmurov, A. S. Naumova, Yu. A. Khoroshutina, A. Yu. Sukhorukov, S. L. Ioffe, “Stereoselective synthesis of spirocyclic nitronates by SnCl4-promoted reaction of nitroalkenes with C-2 substituted 4-methylidene-1,3-dioxolane”, Mendeleev Commun., 25:6 (2015), 449–451
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc2441
https://www.mathnet.ru/rus/mendc/v25/i6/p449
Эта публикация цитируется в следующих 9 статьяx:
Max M. Majireck, John M. Bennett, Comprehensive Heterocyclic Chemistry IV, 2022, 283
Ewa Dresler, Agnieszka Kącka-Zych, Magdalena Kwiatkowska, Radomir Jasiński, “Regioselectivity, stereoselectivity, and molecular mechanism of [3 + 2] cycloaddition reactions between 2-methyl-1-nitroprop-1-ene and (Z)-C-aryl-N-phenylnitrones: a DFT computational study”, J Mol Model, 24:11 (2018)
Vladimir A. Motornov, Vasiliy M. Muzalevskiy, Andrey A. Tabolin, Roman A. Novikov, Yulia V. Nelyubina, Valentine G. Nenajdenko, Sema L. Ioffe, “Radical Nitration-Debromination of α-Bromo-α-fluoroalkenes as a Stereoselective Route to Aromatic α-Fluoronitroalkenes—Functionalized Fluorinated Building Blocks for Organic Synthesis”, J. Org. Chem., 82:10 (2017), 5274
V. A. Egorov, L. S. Khasanova, F. A. Gimalova, A. N. Lobov, M. S. Miftakhov, “Straightforward synthesis of pyrrolizidines”, Mendeleev Commun., 27:2 (2017), 163–165
Oleg V. Fedorov, Vitalij V. Levin, Alexander D. Volodin, Marina I. Struchkova, Alexander A. Korlyukov, Alexander D. Dilman, “Synthesis of difluorosubstituted six-membered nitronates via an addition/substitution cascade”, Tetrahedron Letters, 57:32 (2016), 3639
Yana A. Naumovich, Victoria Emily Buckland, Dmitry A. Sen'ko, Yulia V. Nelyubina, Yulia A. Khoroshutina, Alexey Yu. Sukhorukov, Sema L. Ioffe, “Metal-assisted addition of a nitrate anion to bis(oxy)enamines. A general approach to the synthesis of α-nitroxy-oxime derivatives from nitronates”, Org. Biomol. Chem., 14:16 (2016), 3963
N. V. Orlov, “Rational design of complex molecular structures starting from readily available precursors”, Russ Chem Bull, 65:6 (2016), 1418
Alexey Yu. Sukhorukov, Anna A. Sukhanova, Sergei G. Zlotin, “Stereoselective reactions of nitro compounds in the synthesis of natural compound analogs and active pharmaceutical ingredients”, Tetrahedron, 72:41 (2016), 6191
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
Обратная связь: