Аннотация:
The Friedel–Crafts reaction between electron-rich (het)arenes and β-nitrostyrenes under MgI2 or Ca(NTf2)2 catalysis affords 1-(het)aryl-2-nitro-1-phenylethanes in yields up to 94%.
Образец цитирования:
M. N. Feofanov, A. D. Averin, I. P. Beletskaya, “Friedel–Crafts reaction of electron-rich (het)arenes with nitroalkenes”, Mendeleev Commun., 29:2 (2019), 138–139
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc1447
https://www.mathnet.ru/rus/mendc/v29/i2/p138
Эта публикация цитируется в следующих 5 статьяx:
Periklis X. Kolagkis, Eirini M. Galathri, Christoforos G. Kokotos, “Light-driven Michael addition of indoles to β-nitroolefins in aqueous medium”, Catalysis Today, 441 (2024), 114868
Amjad Ali, Raveena Jajoria, Harish K. Harit, Ravi P. Singh, “Diastereoselective 1,6-Addition of α-Phosphonyloxy Enolates to para-Quinone Methides”, J. Org. Chem., 87:8 (2022), 5213
Shui-Li Liu, Qi-Wei Chen, Zhen-Wei Zhang, Qing Chen, Lian-Qiang Wei, Ning Lin, “Efficient heterogeneous catalyst of Fe(II)-based coordination complexes for Friedel-Crafts alkylation reaction”, Journal of Solid State Chemistry, 310 (2022), 123045
Alessandro Palmieri, Marino Petrini, “Synthesis and practical applications of 2-(2-nitroalkyl)pyrroles”, Org. Biomol. Chem., 18:24 (2020), 4533
Aleksei G. Gladyshkin, Aleksei B. Sheremetev, “An unusual Fluorodinitroethylation Reaction of 3-Azidopyrazole”, Chem Heterocycl Comp, 55:8 (2019), 779
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