Synthesis of 2'-deoxyribonucleoside derivatives of 1-deazapurine

Article abstract of DOI:10.1080/15257779408013282

5,7-Dichloro-3H-imidazo[4,5-b]pyridine (4) is a versatile base which can be coupled with a variety of sugar moieties and transformed in a series of 7- alkyl(aryl)amino-derivatives by reacting with the corresponding amines. In this paper synthesis, structure elucidation and ADA inhibitory activity of 2'-deoxyribonucleoside derivatives of N⁶-substituted 1-deazaapurines are described.

Full text of DOI:10.1080/15257779408013282

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Nucleosides and Nucleotides
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Synthesis of 2′-Deoxyribonucleoside
Derivatives of 1-Deazapurine
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G. Cristalli , S. Vittori , A. Eleuteri , R. Volpini , E. Camaioni
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G. Lupidi
Dipartimento di Scienze Chimiche and Dipartimento di biologia
Cellulare , Università di Camerino , 62032, Camerino, Italy
Published online: 23 Sep 2006.
To cite this article: G. Cristalli , S. Vittori , A. Eleuteri , R. Volpini , E. Camaioni & G. Lupidi (1994)
Synthesis of 2′-Deoxyribonucleoside Derivatives of 1-Deazapurine, Nucleosides and Nucleotides,
13:1-3, 835-848, DOI: 10.1080/15257779408013282
To link to this article: http://dx.doi.org/10.1080/15257779408013282
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