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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 6 scientific papers (total in 6 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 (6)
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.
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
Linking options:
  • https://www.mathnet.ru/eng/mendc4776
  • https://www.mathnet.ru/eng/mendc/v7/i2/p48
  • This publication is cited in the following 6 articles:
    1. Leonid N. Koikov, Mingming Han, Dawn M. Wellman, Jim A. Kelly, Irina P. Smoliakova, “The Use oftert-Butyl Vinyl Ether in Stepwise Electrophilic Addition Reactions”, Synthetic Communications, 30:18 (2000), 3451  crossref
    2. Irina P. Smoliakova, Mingming Han, Jianchun Gong, Ron Caple, William A. Smit, “Reaction of vinyl ethers with ArSCl adducts of d-glucal”, Tetrahedron, 55:15 (1999), 4559  crossref
    3. M. I. Lazareva, Yu. K. Kryschenko, R. Caple, V. G. YoungJr, W. A. Smit, “Highly diastereocelective one-pot four-component coupling of p-TolSCI, 1-methoxycycloalkene, methyl vinyl ether and a carbon nucleophile leading to the synthesis of polyfunctional compounds”, Mendeleev Commun., 9:1 (1999), 24–25  mathnet  crossref
    4. M. I. Lazareva, Yu. K. Kryschenko, A. D. Dilman, A. Hayford, R. Caple, W. A. Smit, “Four-component couplingvia a sequence of threeAd E reactions involving arenesulfenyl chloride, two alkyl vinyl ether units, and silicon-containing π-donors as a method for the synthesis of polyfunctional compounds”, Russ Chem Bull, 47:5 (1998), 895  crossref
    5. A. HAYFORD, M. LOVDAHL, M. I. LAZAREVA, YU. K. KRYSCHENKO, T. JOHNSON, A. D. DILMAN, I. P. SMOLIAKOVA, R. CAPLE, W. A. SMIT, “ChemInform Abstract: Trimethylsilyl Derivatives as Final Nucleophiles in the Tandem Sequence of an ArSCl‐Initiated AdE Reaction Resulting in the Synthesis of Polyfunctional Compounds.”, ChemInform, 28:38 (1997)  crossref
    6. M. I. Lazareva, Yu. K. Kryschenko, R. Caple, W. A. Smit, K. A. Lyssenko, A. S. Shashkov, “Diastereoselective synthesis of polyfunctional compounds based on the tandem sequence of threeAd E reactions using cyclic vinyl ethers as first alkene components”, Russ Chem Bull, 49:1 (1990), 85  crossref
    Citing articles in Google Scholar: Russian citations, English citations
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