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

Authors

  • А. Н. Кравченко Институт органической химии им. Н. Д. Зелинского РАН
  • И. Е. Чикунов Институт органической химии им. Н. Д. Зелинского РАН
  • К. А. Лысенко Институт элементоорганических соединений им. А. Н. Несмеянова РАН
  • В. В. Баранов Институт органической химии им. Н. Д. Зелинского РАН

DOI:

https://doi.org/10.1007/1858

Keywords:

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

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

 

Author Biography

А. Н. Кравченко, Институт органической химии им. Н. Д. Зелинского РАН

Ангелина Николаевна Кравченко

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Published

2014-09-30

Issue

No. 9 (2014)

Section

Original Papers