The synthesis of bicyclic nucleosides related to uridine, 4-(β-D-ribofuranosyl)thiazolo[5,4-d]pyrimidines

Abstract
The silyl alkylation procedure has furnished the first thiazolo [5,4-d]pyrimidine nucleoside (both α and β anomers isolated and characterized), and the site of alkylation has been established by a comparison of the u.v. spectra of the nucleoside and model N-methyl compounds.

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