Issue 5, 2001
From the journal:

Mendeleev Communications

Selectivity of the Lewis acid-induced transformations of polyfunctional compounds containing a 4,6-dialkoxy-7-(arylthio)heptene moiety

Dmitrii S. Chekmaev,   Andrei V. Maskaev,   Georgy V. Zatonsky,   Margarita I. Lazareva,   Ron Caple  and  William A. Smit  

Abstract

The interaction of the title adducts with Lewis acids may proceed as an attack at either β-alkoxy or δ-alkoxy group to the arylthio substituent leading to the formation of substituted cyclohexane or 1,3-diene derivatives, respectively.

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Article information

DOI
https://doi.org/10.1070/MC2001v011n05ABEH001513
Article type
Paper

Mendeleev Commun., 2001,11, 176-178

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Selectivity of the Lewis acid-induced transformations of polyfunctional compounds containing a 4,6-dialkoxy-7-(arylthio)heptene moiety

D. S. Chekmaev, A. V. Maskaev, G. V. Zatonsky, M. I. Lazareva, R. Caple and W. A. Smit, Mendeleev Commun., 2001, 11, 176 DOI: 10.1070/MC2001v011n05ABEH001513

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