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Hydrosilylation of N-allylpyrrolidine and N-allylpiperidine

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

It was found that the hydrosilylation of N-allylpyrrolidine and N-allylpiperidlne by trialkylsilanes, triethoxysilane, and 3H-heptamethyltrisiloxane in the presence of H2PtCl6 · 6H2O proceeds to form γ -adducts.

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Literature cited

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Authors and Affiliations

  1. Institute of Organic Synthesis, Academy of Sciences of the Latvian SSR, Riga

    É. Ya. Lukevits, A. E. Pestunovich, M. G. Voronkov & T. M. Kupch

Authors
  1. É. Ya. Lukevits
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  2. A. E. Pestunovich
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  3. M. G. Voronkov
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  4. T. M. Kupch
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Additional information

Communication XXXII from the series “Nitrogen-Containing Organosilicon Compounds.” See [1] for communication XXXI.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 485–487, April, 1972.

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Lukevits, É.Y., Pestunovich, A.E., Voronkov, M.G. et al. Hydrosilylation of N-allylpyrrolidine and N-allylpiperidine. Chem Heterocycl Compd 8, 442–444 (1972). https://doi.org/10.1007/BF00477419

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  • DOI: https://doi.org/10.1007/BF00477419

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