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Telomerization of vinyl chloride by methyl methoxyacetate

Bulletin of the Academy of Sciences of the USSR, Division of chemical science volume 37, pages 1714–1717 (1988)Cite this article

Conclusions

The telomerization of vinyl chloride by methyl methoxyacetate proceeds due to cleavage of the α-C-H and methoxy group C-H bonds in the telogen and is accompanied by rearrangement of the radicals with 1,5-hydrogen migration.

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Literature cited

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Authors and Affiliations

  1. A. N. Nesmeyanov Institute of Heteroorganic Compounds, Academy of Sciences of the USSR, Moscow

    N. S. Ikonnikov & A. B. Terent'ev

Authors
  1. N. S. Ikonnikov
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  2. A. B. Terent'ev
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 8, pp. 1914–1917, August, 1988.

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Ikonnikov, N.S., Terent'ev, A.B. Telomerization of vinyl chloride by methyl methoxyacetate. Russ Chem Bull 37, 1714–1717 (1988). https://doi.org/10.1007/BF00961133

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  • DOI: https://doi.org/10.1007/BF00961133

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