Chemistry of Heterocyclic Compounds

, Volume 41, Issue 10, pp 1205–1236

Kost-Sagitullin Rearrangement and Other Isomerization Recyclizations of Pyrimidines. (Review)

  • G. G. Danagulyan
Article

DOI: 10.1007/s10593-005-0308-z

Cite this article as:
Danagulyan, G.G. Chem Heterocycl Compd (2005) 41: 1205. doi:10.1007/s10593-005-0308-z

Abstract

Data on the isomerization recyclizations of pyrimidines, particularly the Kost-Sagitullin and other transformations accompanied by substitution of an endocyclic atom in pyrimidine by an extracyclic nitrogen or carbon atom (N-N, N-C, or C-C recyclizations), are summarized and analyzed. Data from research on the Kost-Sagitullin and certain other isomerization transformations of pyrimidines at the Institute of Organic Chemistry, National Academy of Sciences of the Republic of Armenia, in recent years are presented.

Keywords

1,2-dialkylpyrimidinium iodides pyrazolo[1,5-a]pyrimidine pyrimidine isomerization nucleophilic rearrangements recyclization 

Copyright information

© Springer Science+Business Media, Inc. 2005

Authors and Affiliations

  • G. G. Danagulyan
    • 1
  1. 1.Institute of Organic ChemistryNational Academy of Sciences of the Republic of ArmeniaErevanArmenia

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