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Mendeleev Communications, 2019, Volume 29, Issue 1, Pages 57–58
DOI: https://doi.org/10.1016/j.mencom.2019.01.018 (Mi mendc1420) 		 
This article is cited in 5 scientific papers (total in 5 papers)

Communications

Diastereoselective vinylogous Mannich reaction of perfluoroalkylated cyclic imines with 2-trimethylsilyloxyfuran

O. I. Shmatova, V. G. Nenajdenko

Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation
Full-text PDF (275 kB) Citations (5) Supplementary materials
DOI: https://doi.org/10.1016/j.mencom.2019.01.018
Abstract: The reaction between 2-trimethylsilyloxyfuran and perfluoroalkylated cyclic ketimines with different ring sizes affords 5-(2-perfluoroalkyl-1-azacycloalk-2-yl)furan-2(5H)-ones in yields up to 89% and with excellent rel-(R,R)-diastereoselectivity.
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Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (570.8 Kb)


Citation: O. I. Shmatova, V. G. Nenajdenko, “Diastereoselective vinylogous Mannich reaction of perfluoroalkylated cyclic imines with 2-trimethylsilyloxyfuran”, Mendeleev Commun., 29:1 (2019), 57–58
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  • https://www.mathnet.ru/eng/mendc1420
  • https://www.mathnet.ru/eng/mendc/v29/i1/p57
    • This publication is cited in the following 5 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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