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13C NMR spectra of biologically active compounds.

VII. Stereoisomers of cyclopropanecarboxylic esters of the pyrethroid series

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Abstract

The13C spectra of 25 new substituted cyclopropanes of the pyrethoid series have been investigated and a stereochemical assignment has been made of the stereoisomers formed. As the criterion for stereochemical assignment it is proposed to use the values of the chemical shifts for the α-carbon atoms of the substituents in the cyclopropane ring.

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Authors
  1. L. M. Khalilov
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  2. A. A. Fatykhov
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  3. V. S. Sultanova
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  4. F. Z. Makaev
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  5. F. Z. Galin
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  6. G. A. Tolstikov
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  7. A. A. Panasenko
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Additional information

Institute of Chemistry, Bashkir Branch, USSR Academy of Sciences, Ufa. Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 266–272, March–April, 1989.

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Khalilov, L.M., Fatykhov, A.A., Sultanova, V.S. et al. 13C NMR spectra of biologically active compounds.. Chem Nat Compd 25, 231–236 (1989). https://doi.org/10.1007/BF00598419

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  • DOI: https://doi.org/10.1007/BF00598419

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