Issue 2, 1997

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

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.

Article information

Article type
Paper

Mendeleev Commun., 1997,7, 48-50

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

A. Hayford, M. Lovdahl, M. I. Lazareva, Y. K. Kryschenko, T. Johnson, A. D. Dilman, I. P. Smoliakova, R. Caple and W. A. Smit, Mendeleev Commun., 1997, 7, 48 DOI: 10.1070/MC1997v007n02ABEH000726

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