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


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详细

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.

作者简介

V. Musiyak

Postovskii Institute of Organic Synthesis, Ural Branch

Email: ca@ios.uran.ru
俄罗斯联邦, Yekaterinburg

I. Nizova

Postovskii Institute of Organic Synthesis, Ural Branch

Email: ca@ios.uran.ru
俄罗斯联邦, Yekaterinburg

T. Matveeva

Postovskii Institute of Organic Synthesis, Ural Branch

Email: ca@ios.uran.ru
俄罗斯联邦, Yekaterinburg

G. Levit

Postovskii Institute of Organic Synthesis, Ural Branch

Email: ca@ios.uran.ru
俄罗斯联邦, Yekaterinburg

V. Krasnov

Postovskii Institute of Organic Synthesis, Ural Branch

编辑信件的主要联系方式.
Email: ca@ios.uran.ru
俄罗斯联邦, Yekaterinburg

V. Charushin

Postovskii Institute of Organic Synthesis, Ural Branch

Email: ca@ios.uran.ru
俄罗斯联邦, Yekaterinburg

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