Volume 33, Issue 35
Natural Products
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ChemInform Abstract: Synthesis, Antiviral and Cytostatic Activities, of Carbocyclic Nucleosides Incorporating a Modified Cyclopentane Ring. Part 4. Adenosine and Uridine Analogues.

M. Isabel Nieto

M. Isabel Nieto

Dep. Quim. Org., Fac. Farm., Univ. Santiago de Compostela, E-15782 Santiago de Compostela, Spain

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Olga Caamano

Olga Caamano

Dep. Quim. Org., Fac. Farm., Univ. Santiago de Compostela, E-15782 Santiago de Compostela, Spain

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Franco Fernandez

Franco Fernandez

Dep. Quim. Org., Fac. Farm., Univ. Santiago de Compostela, E-15782 Santiago de Compostela, Spain

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Maria Gomez

Maria Gomez

Dep. Quim. Org., Fac. Farm., Univ. Santiago de Compostela, E-15782 Santiago de Compostela, Spain

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Jan Balzarini

Jan Balzarini

Dep. Quim. Org., Fac. Farm., Univ. Santiago de Compostela, E-15782 Santiago de Compostela, Spain

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Erik De Clercq

Erik De Clercq

Dep. Quim. Org., Fac. Farm., Univ. Santiago de Compostela, E-15782 Santiago de Compostela, Spain

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First published: 20 May 2010

Abstract

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

ChemInform Abstract

New carbocyclic nucleosides are prepared by mounting a purine [cf. (V), (VI), (VII)], 8-azapurine [cf. (VIII), (IX)] or pyrimidine [cf. (XII), (XIII)] on the amino group of the aminoalcohol (I). The products are evaluated as antiviral and antitumor agents. Only purine derivative (V) displays any cytostatic activity.

chemical structure image

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