Аннотация:
3-Aryl-4-methylpyrrole-2-carboxylates were prepared via the Barton–Zard reaction using pseudonitrosites as a source of the corresponding nitroalkenes. The starting pseudonitrosites were, in turn, obtained via addition of N2O3 to propenylbenzenes available from the natural plant essential oils.
Образец цитирования:
D. A. Rusanov, A. B. Myshlyavtsev, E. A. Silyanova, A. V. Samet, V. V. Semenov, “Pseudonitrosites as masked nitroalkenes in the Barton–Zard pyrrole synthesis”, Mendeleev Commun., 30:4 (2020), 485–486
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc1231
https://www.mathnet.ru/rus/mendc/v30/i4/p485
Эта публикация цитируется в следующих 2 статьяx:
Ilya V. Efimov, Larisa N. Kulikova, Almira R. Miftyakhova, Maria D. Matveeva, Leonid G. Voskressensky, “Recent Advances for the Synthesis of N‐Unsubstituted Pyrroles”, ChemistrySelect, 6:48 (2021), 13740
Daniil А. Rusanov, Alexander V. Samet, Vyacheslav V. Rusak, Victor V. Semenov, “Synthesis of functionalized 1-methylchromeno[3,4-b]pyrrol-4(3H)-ones via the Barton–Zard reaction starting from pseudonitrosites”, Chem Heterocycl Comp, 57:9 (2021), 944
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