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Mendeleev Communications, 1996, Volume 6, Issue 4, Pages 150–151
DOI: https://doi.org/10.1070/MC1996v006n04ABEH000621
(Mi mendc4955)
 

This article is cited in 1 scientific paper (total in 1 paper)

Synthesis of substituted 2- and (4-alkoxyphenyl)trichlorostannanes. A novel method of preparative cleavage of the Si–C bond

I. M. Lazareva, G. V. Dolgushina, V. P. Feshinb, M. G. Voronkova

a A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk, Russian Federation
b Institute of Technical Chemistry, Ural Branch of the Russian Academy of Sciences, Perm, Russian Federation
Full-text PDF (212 kB) Citations (1)
Abstract: The reaction of ortho- and para-(alkoxyaryl)trimethylsilanes with tin tetrachloride proceeds under mild conditions with cleavage of the Si–C bond and formation of the corresponding stannanes.
Document Type: Article
Language: English


Citation: I. M. Lazarev, G. V. Dolgushin, V. P. Feshin, M. G. Voronkov, “Synthesis of substituted 2- and (4-alkoxyphenyl)trichlorostannanes. A novel method of preparative cleavage of the Si–C bond”, Mendeleev Commun., 6:4 (1996), 150–151
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  • This publication is cited in the following 1 articles:
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