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

G. G. Danagulyan

doi:10.1007/s10593-005-0308-z

Chemistry of Heterocyclic Compounds

October 2005, Volume 41, Issue 10, pp 1205–1236

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

Authors
Authors and affiliations

G. G. Danagulyan

Article

Received:: 06 May 2005

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

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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

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1.Institute of Organic ChemistryNational Academy of Sciences of the Republic of ArmeniaErevanArmenia

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

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