Synthesis of New Purine Derivatives Containing α- and ω-Amino Acid Fragments


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Resumo

New conjugates of purine and 2-aminopurine with several α- and ω-amino acids have been synthesized following two approaches based on the condensation and nucleophilic substitution reactions. The enantiomeric purity of the isolated compounds has been confirmed by reversed-phase HPLC using a chiral stationary phase to demonstrate the absence of racemization during the synthesis. The conjugates are inactive against Mycobacterium tuberculosis H37Rv.

Sobre autores

V. Musiyak

Postovskii Institute of Organic Synthesis, Ural Branch

Email: ca@ios.uran.ru
Rússia, Yekaterinburg

I. Nizova

Postovskii Institute of Organic Synthesis, Ural Branch

Email: ca@ios.uran.ru
Rússia, Yekaterinburg

T. Matveeva

Postovskii Institute of Organic Synthesis, Ural Branch

Email: ca@ios.uran.ru
Rússia, Yekaterinburg

G. Levit

Postovskii Institute of Organic Synthesis, Ural Branch

Email: ca@ios.uran.ru
Rússia, Yekaterinburg

V. Krasnov

Postovskii Institute of Organic Synthesis, Ural Branch

Autor responsável pela correspondência
Email: ca@ios.uran.ru
Rússia, Yekaterinburg

V. Charushin

Postovskii Institute of Organic Synthesis, Ural Branch

Email: ca@ios.uran.ru
Rússia, Yekaterinburg

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