Conclusions
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1.
The disubstituted double bond in theβ-position with respect to the silicon atom does not enter into the hydroalumination reaction because of the interaction of theπ-electrons with the 3d-vacant orbitale of the silicon atom.
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2.
The disubstituted double bond, which is removed from the silicon atom, enters into the hydro-alumination reaction without a shift in the vinyl position to form organoaluminum compounds which contain the silicon atom.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 4, pp. 866–869, April, 1976.
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Yur'ev, V.P., Gailyunas, G.A., Yusupova, F.G. et al. The hydroalumination reaction for some alkenyltrimethylsilanes with diisobutylaluminum hydride. Russ Chem Bull 25, 844–847 (1976). https://doi.org/10.1007/BF00922394
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DOI: https://doi.org/10.1007/BF00922394