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., 1997, Volume 7, Issue 2,Pages <nobr>48

This article is cited 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. Hayford^a, M. Lovdahl^a, M. I. Lazareva^b, Yu. K. Kryschenko^a, T. Johnson^a, A. D. Dilman^c, I. P. Smoliakova^d, R. Caple^a, W. A. Smit^b

^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

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.

Language: English

DOI: 10.1070/MC1997v007n02ABEH000726