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Unusual transfoemation of trimethylsilyl ester of 5-chloromethyl-2-isoxazoline-3-carboxylic acid

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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Conclusions

The silylation of 5-chloromethyl-2-isoxazoline-3-carboxylic acid with the usual silylating agents leads to the corresponding trimethylsilyl ester, which when heated is converted to 4-chloro-3-trimethylsiloxybutyronitrile.

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Literature cited

  1. R. Rambaud and M. Vesierre, Bull. Soc. Chim. France,1956, 783.

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Authors and Affiliations

  1. N. D. Zelinskii Institute of Organic Chemistry, Academy of Sciences of the USSR, Moscow

    S. L. Ioffe, Yu. D. Kuznetsov & V. A. Tartakovskii

Authors
  1. S. L. Ioffe
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  2. Yu. D. Kuznetsov
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  3. V. A. Tartakovskii
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 12, pp. 2818–2819, December, 1981.

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Ioffe, S.L., Kuznetsov, Y.D. & Tartakovskii, V.A. Unusual transfoemation of trimethylsilyl ester of 5-chloromethyl-2-isoxazoline-3-carboxylic acid. Russ Chem Bull 30, 2350–2351 (1981). https://doi.org/10.1007/BF00963710

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  • DOI: https://doi.org/10.1007/BF00963710

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