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Mendeleev Communications, 1997, Volume 7, Issue 2, Pages 48–50
DOI: https://doi.org/10.1070/MC1997v007n02ABEH000726
(Mi mendc4776)
 

This article is cited in 7 scientific papers (total in 7 papers)

Trimethylsilyl derivatives as final nucleophiles in the tandem sequence of an ArSCl-initiated AdE reaction resulting in the synthesis of polyfunctional compounds

A. Hayforda, M. Lovdahla, M. I. Lazarevab, Yu. K. Kryschenkoa, T. Johnsona, A. D. Dilmanc, I. P. Smoliakovad, R. Caplea, W. A. Smitb

a Department of Chemistry, University of Minnesota Duluth, Duluth, Minnesota, USA
b N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
c Higher Chemical College of the Russian Academy of Sciences, D.I. Mendeleev University of Chemical Technology of Russia, Moscow, Russian Federation
d Department of Chemistry, University of North Dakota, Grand Forks, North Dakota, USA
Full-text PDF (69 kB) Citations (7)
Abstract: The use of allyl silanes and silyl vinyl ethers in the final step of a Lewis acid-mediated sequence involving reaction of ArSCl, two vinyl ether units and a C-nucleophile has been studied, thereby allowing introduction of functional groups into the four-component adduct.
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Document Type: Article
Language: English


Citation: A. Hayford, M. Lovdahl, M. I. Lazareva, Yu. K. Kryschenko, T. Johnson, A. D. Dilman, I. P. Smoliakova, R. Caple, W. A. Smit, “Trimethylsilyl derivatives as final nucleophiles in the tandem sequence of an ArSCl-initiated AdE reaction resulting in the synthesis of polyfunctional compounds”, Mendeleev Commun., 7:2 (1997), 48–50
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  • This publication is cited in the following 7 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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