Reactions of thieno[2,3-с]pyrrolines with dehydrobenzene

[Figure not available: see fulltext.] Thieno[2,3-c]pyrrolines bearing a branched substituent at the nitrogen atom reacted with dehydrobenzene, furnishing thienylaziridines. N-Benzyl-substituted thienopyrroline under the reaction conditions gave a Stevens rearrangement product, 6-benzyl-5-phenylthieno[2,3-c]-pyrroline. © 2018, Springer Science+Business Media, LLC, part of Springer Nature.

Авторы
Издательство
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Номер выпуска
6
Язык
Английский
Страницы
664-668
Статус
Опубликовано
Том
54
Год
2018
Организации
  • 1 RUDN University, 6 Miklukho-Maklaya St., Moscow, 117198, Russian Federation
  • 2 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky Ave., Moscow, 119991, Russian Federation
Ключевые слова
dehydrobenzene; Stevens rearrangement; thieno[2,3-c]pyrrolines; thienyl-substituted aziridines
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