Summary
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1.
In diene condensations with cyclones, trimethylvinyltin reacts the most readily and triphenylvinyltin the least readily.
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2.
New cyclic organotin compounds were obtained as the result of the reaction of phencyclone with vinyltln compounds.
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3.
The reactions of vinyltin compounds with tetracyclone and with acecyclone occur with elimination of the endo-carbonyl bridge and the tin-containing side chain.
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Arbuzov, B.A., Shapshinskaya, L.A. & Kudryavtseva, M.I. Vinyltin compounds in diene synthesis with cyclones. Russ Chem Bull 10, 2020–2022 (1961). https://doi.org/10.1007/BF01182945
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DOI: https://doi.org/10.1007/BF01182945