Michael addition to 3-(2-nitrovinyl)indoles – route toward aliphatic nitro compounds with heterocyclic substituents

[Figure not available: see fulltext.] Synthetic approach toward indole derivatives bearing 2-nitroethyl group and polar azole moiety has been developed. This method involves conjugate addition of 1,3-dicarbonyl compounds to 3-(2-nitrovinyl)-1H-indoles followed by cyclocondensation with hydrazine or hydroxylamine to furnish pyrazole or isoxazole ring. Application of microwave activation allows to obtain the target indole derivatives in short time and avoid protection of indole nitrogen atom. © 2019, Springer Science+Business Media, LLC, part of Springer Nature.

Авторы
Aksenov N.A. 1 , Skomorokhov A.A.1 , Aksenov A.V. 1 , Voskressensky L.G. 2 , Rubin M.A.1, 3
Издательство
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Номер выпуска
6
Язык
Английский
Страницы
541-546
Статус
Опубликовано
Том
55
Год
2019
Организации
  • 1 North-Caucasus Federal University, 1a Pushkina St., Stavropol, 355009, Russian Federation
  • 2 RUDN University, 6 Miklukho-Maklaya St., Moscow, 117198, Russian Federation
  • 3 The University of Kansas, 1567 Irving Hill Rd, Lawrence, KS 66045-7582, United States
Ключевые слова
indole; isoxazole; Michael addition; microwave-assisted synthesis; nitroalkene; pyrazole
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