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Chemistry of Heterocyclic Compounds

, Volume 20, Issue 11, pp 1200–1202 | Cite as

Epoxidation of 2-aryl-4-methyl-3,6-dihydropyrans and reaction of the products with piperidine

  • U. G. Ubatullin
  • L. V. Syurina
  • S. A. Vasil'eva
  • T. B. Semenov
  • M. G. Safarov
Article
  • 28 Downloads

Abstract

2-Aryl-4-methyl-4,5-epoxytetrahydropyrans, which react with piperidine regioselectively with trans-diaxial cleavage of the oxide ring at the least substituted carbon atom, were synthesized by the reaction of 2-aryl-4-methyl-3,6-dihydropyrans with peracids.

Keywords

Oxide Organic Chemistry Carbon Atom Epoxidation Piperidine 
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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Copyright information

© Plenum Publishing Corporation 1985

Authors and Affiliations

  • U. G. Ubatullin
    • 1
  • L. V. Syurina
    • 1
  • S. A. Vasil'eva
    • 1
  • T. B. Semenov
    • 1
  • M. G. Safarov
    • 1
  1. 1.Bashkir State UniversityUfa

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