Nucleophilic substitution or dipolar 1,3-cycloaddition in reactions of cyanamide with 4-arylpyrimidine 1-oxides View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2003-05

AUTHORS

A. M. Prokhorov, D. N. Kozhevnikov, V. L. Rusinov, O. N. Chupakhin

ABSTRACT

Pyrimidine 1-oxides with cyanamide afforded 2-ureidopyrimidines as the result of the nucleophilic substitution of hydrogen, whereas the formation of similar 2-trichloroacetylaminopyrimidines occurs as dipolar 1,3-cycloaddition of the same oxides to trichloroacetonitrile under much more drastic conditions and in lower yields.

PAGES

1195-1197

Journal

TITLE

Russian Chemical Bulletin

ISSUE

5

VOLUME

52

Author Affiliations

Identifiers

URI

http://scigraph.springernature.com/pub.10.1023/a:1024729912415

DOI

http://dx.doi.org/10.1023/a:1024729912415

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1041116530


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