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Chemistry of Heterocyclic Compounds

, Volume 10, Issue 3, pp 276–279 | Cite as

Research on furan acetal compounds

VII. PMR spectra, configuration, and conformations of substituted 2-(α-furyl)-1,3-diozanes
  • Yu. Yu. Samitov
  • Z. I. Zelikman
  • A. I. Shkrebets
  • V. G. Kul'nevich
Article
  • 26 Downloads

Abstract

The configuration and preferred conformations of a number of stereoisomeric 2-(α-furyl) 1,3-dioxanes were established by PMR spectroscopy. It is shown that cis orientation of the NO2 groups with respect to the furyl ring is primarily realized for 2-(α'-nitro-α-furyl)-5-ethyl-5-nitro-1,3-dioxanes.

Keywords

Spectroscopy Acetal Organic Chemistry Furan Furyl 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Literature cited

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    V. G. Kul'nevich, Z. I. Zelikman, A. I. Shkrebets, B. A. Tertov, and M. M. Ketslakh, Khim. Geterotsikl. Soedin., 595 (1973).Google Scholar
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    Z. I. Zelikman, A. I. Shkrebets, V. G. Kul'nevich, and B. A. Tertov, Khim. Geterotsikl. Soedin., 438 (1971).Google Scholar
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    Yu. Yu. Samitov, Dokl. Akad. Nauk SSSR, 164, No. 2, 347 (1965).Google Scholar

Copyright information

© Plenum Publishing Corporation 1975

Authors and Affiliations

  • Yu. Yu. Samitov
    • 1
  • Z. I. Zelikman
    • 1
  • A. I. Shkrebets
    • 1
  • V. G. Kul'nevich
    • 1
  1. 1.Krasnodar Polytechnical InstituteV. I. Ul'yanov-Lenin Kazan State UniversityUSSR

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