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Chemistry of Heterocyclic Compounds

, Volume 10, Issue 8, pp 951–952 | Cite as

Nitration of 2- and 5-benzyl-3-hydroxypyridines and their N-oxides

  • L. D. Smirnov
  • V. S. Zhuravlev
  • V. P. Lezina
  • K. M. Dyumaev
Article

Abstract

The nitration of 2- and 5-benzyl-3-hydroxpyridines and their N-oxides takes place in the para position of the phenyl ring. The introduction of an N-oxide group into the Β-pyridol ring does not affect the orientation of substitution.

Keywords

Organic Chemistry Phenyl Nitration Phenyl Ring Para Position 
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.

Literature cited

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    L. D. Smirnov, V. I. Kuz'min, V. P. Lezina, and K. M. Dyumaev, Izv. Akad. Nauk SSSR, Ser Khim., 1897 (1970).Google Scholar

Copyright information

© Plenum Publishing Corporation 1976

Authors and Affiliations

  • L. D. Smirnov
    • 1
  • V. S. Zhuravlev
    • 1
  • V. P. Lezina
    • 1
  • K. M. Dyumaev
    • 1
  1. 1.Institute of Chemical PhysicsAcademy of Sciences of the USSRMoscow

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