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GLYCOLURILS IN α-UREIDO- AND α-AMINOALKYLATION REACTIONS. 3. N-(HYDROXYMETHYL)GLYCOLURILS IN REACTIONS WITH ALIPHATIC AMINES AND AMINO ACIDS

А. Н. Кравченко, И. Е. Чикунов, К. А. Лысенко, В. В. Баранов
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Abstract


The condensation of aliphatic alkylamines and achiral amino acids with 1,5-butano-2,4,6,8-tetra-(hydroxymethyl)- and 2,4,6,8-tetra(hydroxymethyl)glycolurils was used to prepare and characterize polycyclic condensed compounds (including some previously unknown examples) containing  glycoluril and alkylamine fragments. X-ray structural study of the obtained compounds was used to identify n(N)→ s(C–H) anomeric interaction.

How to Cite
Kravchenko, A. N.; Chikunov, I. E.; Lyssenko, K. A.; Baranov, V. V. Chem. Heterocycl. Compd. 2014, 50, 1322. [Khim. Geterotsikl. Soedin. 2014, 1434.]

For this article in the English edition see DOI 10.1007/s10593-014-1595-z

 


Keywords


alkylamines; amino acids; condensed tri-, tetra-, and pentacyclic systems; ethanolamine; hydroxymethyl-substituted glycolurils; condensation; X-ray structural analysis

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