Аннотация:
The reaction of o-phenylenediamine with 2-alkoxypropenals at room temperature affords 2-(1-alkoxyvinyl)benzimidazoles (53–68%), while 2-hydroxy-3-arylpropenals give 2-(arylmethyl) quinoxalines (85–86%).
Образец цитирования:
N. V. Vchislo, E. A. Verochkina, L. I. Larina, A. V. Vashchenko, Yu. A. Chuvashev, “Reaction of 2-alkoxy- and 2-hydroxypropenals with o-phenylenediamine: a route to benzimidazoles and quinoxalines”, Mendeleev Commun., 27:2 (2017), 166–168
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc1932
https://www.mathnet.ru/rus/mendc/v27/i2/p166
Эта публикация цитируется в следующих 4 статьяx:
N. V. Vchislo, V. G. Fedoseeva, V. V. Novokshonov, L. I. Larina, I. B. Rosentsveig, E. A. Verochkina, “Synthesis of new alkoxy/alkylthiovinylated oxazoles using tosylmethyl isocyanide”, Mendeleev Commun., 30:3 (2020), 350–351
Lyudmila I. Larina, “Nuclear Quadrupole Resonance Spectroscopy: Tautomerism and Structure of Functional Azoles”, Crystals, 9:7 (2019), 366
M. Milen, T. Szabó, A. Dancsó, P. Ábrányi-Balogh, B. Volk, “Synthesis of 1-aryl-3H-[1,2,5]triazepino[5,4-a]benzimidazol-4(5H)-ones and quantum chemical investigation of the rotamers of the Boc-protected hydrazide key intermediate”, Mendeleev Commun., 29:3 (2019), 294–295
Lyudmila I. Larina, Advances in Heterocyclic Chemistry, 124, 2018, 233
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