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Mendeleev Communications, 2021, Volume 31, Issue 2, Pages 246–247
DOI: https://doi.org/10.1016/j.mencom.2021.03.034
(Mi mendc894)
 

This article is cited in 9 scientific papers (total in 9 papers)

Communications

Different addition modes of cyclopentadiene and furan at methylidene(thio)hydantoins

D. E. Shybanov, M. E. Kukushkin, V. A. Tafeenko, N. V. Zyk, Yu. K. Grishin, V. A. Roznyatovsky, E. K. Beloglazkina

Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation
Full-text PDF (422 kB) Citations (9)
Abstract: 3-Methylidene-5-phenylhydantoin and 3-methylidene-5-phenylthiohydantoin react with cyclopentadiene forming spirocyclic Diels–Alder adducts. In contrast, their reactions with furan in the presence of AlCl3 give the products of the furan α-amidoalkylation.
Keywords: hydantoins, thiohydantoins, Diels–Alder reaction, α-amidoalkylation, X-ray.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (1.1 Mb)


Citation: D. E. Shybanov, M. E. Kukushkin, V. A. Tafeenko, N. V. Zyk, Yu. K. Grishin, V. A. Roznyatovsky, E. K. Beloglazkina, “Different addition modes of cyclopentadiene and furan at methylidene(thio)hydantoins”, Mendeleev Commun., 31:2 (2021), 246–247
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  • https://www.mathnet.ru/eng/mendc/v31/i2/p246
  • This publication is cited in the following 9 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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