The ozonation of 4-thiopyrimidine and 6-thiopurine nucleosides in presence of amines afforded selectively and under mild exptl. conditions several cytidine and adenosine nucleosides. The same reaction carried out in presence of alcs. afforded O4- or O6-alkylated derivs. of the nucleosides.
Ozonation of thionucleosides. A new chemical transformation of 4-thiouracil and 6-thioguanine nucleosides to cytosine and adenosine counterparts / Saladino, R., C., C., F., O., R., N.. - In: TETRAHEDRON. - ISSN 0040-4020. - 51:(1995), pp. 3607-3616. [10.1016/0040-4020(95)00076-K]
Ozonation of thionucleosides. A new chemical transformation of 4-thiouracil and 6-thioguanine nucleosides to cytosine and adenosine counterparts
SALADINO R;
1995
Abstract
The ozonation of 4-thiopyrimidine and 6-thiopurine nucleosides in presence of amines afforded selectively and under mild exptl. conditions several cytidine and adenosine nucleosides. The same reaction carried out in presence of alcs. afforded O4- or O6-alkylated derivs. of the nucleosides.File allegati a questo prodotto
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