Oligodeoxynucleotides embodying the ambiguous base Z, 5-amino-imidazole- 4-carboxamide

Article abstract of DOI:10.1080/15257779508010683

Short oligomers containing 5-amino-1-(2-deoxy-β-D- ribofuranosyl)imidazole -4-carboxamide (dZ) were synthesized in solution using the phosphotriester methodology. Usual acyl groups were used for the canonical bases. For the exocyclic amino function of Z residue, the hydrogenolyzable benzyloxycarbonyl group was introduced.

Full text of DOI:10.1080/15257779508010683

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Nucleosides and Nucleotides
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Oligodeoxynucleotides Embodying
the Ambiguous Base Z, 5-Amino-
imidazole-4-carboxamide
Sylvie Pochet a & Laurence Dugué a
a Unité de Chimie Organique URA CNRS 487, Département de
BGM , Institut Pasteur 28, rue du Docteur Roux 75754, Paris
Cedex, France
Published online: 24 Sep 2006.
To cite this article: Sylvie Pochet & Laurence Dugué (1995) Oligodeoxynucleotides Embodying
the Ambiguous Base Z, 5-Amino-imidazole-4-carboxamide, Nucleosides and Nucleotides, 14:6,
1195-1210, DOI: 10.1080/15257779508010683
To link to this article: http://dx.doi.org/10.1080/15257779508010683
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