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Stereochemistry of cyclic compounds Communication 63. Stereochemistry of the bromination of 4-methyl-cis-4-cyclohexene-1,2-dicarboxylic acid and its anhydride

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

Summary

The stereochemistry of the bromination of 4-methyl-cis-4-cyclohexene-l,2-dicarboxylic acid (I) and its anhydride (II) was studied. The spatial structures of the products were proved, and a possible mechanism scheme for their formation was discussed.

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Literature cited

  1. V. F. Kucherov, A. L. Shabanov, and A. S. Onishchenko, Izv. AN SSSR, Otd. Khim. n., 1963, 844.

  2. A. S. Onishchenko, A. L. Shabanov, and V. F. Kucherov, Izv. AN SSSR, Otd. khim. n., 1963, 852.

  3. K. Crewe, A. Heinke, and Ch. Sommer, Chem. Ber.,89, 1978 (1956).

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  4. A. L. Shabanov, A. S. Onishchenko, and V. F. Kucherov, Izv. AN SSSR, Otd. khim. n., 1963, 1790.

  5. I. N. Nazarov, V. F. Kucherov, and V. M. Andreev, Izv. AN SSSR, Otd. khim. n., 1955, 289; 1956, 951; 1959, 1058.

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This article is published in accordance with a resolution of the Conference of Chief Editors of the Journals of the Academy of Sciences of the USSR, July 12, 1962, as a dissertation paper by A. L. Shabanov.

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Shabanov, A.L., Onishchenko, A.S. & Kucherov, V.F. Stereochemistry of cyclic compounds Communication 63. Stereochemistry of the bromination of 4-methyl-cis-4-cyclohexene-1,2-dicarboxylic acid and its anhydride. Russ Chem Bull 12, 1648–1652 (1963). https://doi.org/10.1007/BF00845794

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  • DOI: https://doi.org/10.1007/BF00845794

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