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.

Authors
Guranova N.I. 1 , Borisova T.N. 1 , Novikov R.A.2 , Sorokina E.A. 1 , Khrustalev V.N. 1 , Varlamov A.V. 1
Journal
Chemistry of Heterocyclic Compounds
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
6
Language
English
Pages
664-668
Status
Published
Link
External link
DOI
10.1007/s10593-018-2324-9
Volume
54
Year
2018
Organizations
  • 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
Keywords
dehydrobenzene; Stevens rearrangement; thieno[2,3-c]pyrrolines; thienyl-substituted aziridines
Date of creation
19.10.2018
Date of change
19.10.2018
Short link
https://repository.rudn.ru/en/records/article/record/6631/
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