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A reaction of tin tetra(N,N-diethylcarbamate) with phenylacetylene as a new route to tetra(phenylethynyl)tin

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Abstract

A reaction of tin tetra(N,N-diethylcarbamate) with phenylacetylene afforded tetra-(phenylethynyl)tin in 77% yield. The reaction can be promoted by Lewis acids.

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Authors and Affiliations

  1. Kuban State University, 149 ul. Stavropol’skaya, 350040, Krasnodar, Russian Federation

    A. S. Levashov, A. A. Andreev, D. S. Buryi & V. V. Konshin

Authors
  1. A. S. Levashov
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  2. A. A. Andreev
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  3. D. S. Buryi
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  4. V. V. Konshin
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Corresponding author

Correspondence to V. V. Konshin.

Additional information

Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 3, pp. 0775–0776, March, 2014.

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Levashov, A.S., Andreev, A.A., Buryi, D.S. et al. A reaction of tin tetra(N,N-diethylcarbamate) with phenylacetylene as a new route to tetra(phenylethynyl)tin. Russ Chem Bull 63, 775–776 (2014). https://doi.org/10.1007/s11172-014-0508-8

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  • DOI: https://doi.org/10.1007/s11172-014-0508-8

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