On the influence of the nature of 2-n-protecting ACYL groups on the stability of deoxyguanosine derivatives

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Abstract

Acid mediated variations of 13C-NMR chemical shifts and destruction kinetics of protected deoxyguanosine derivatives indicate a pronounced effect of the electronegativity of the protecting groups on their stability.

Original languageEnglish
Pages (from-to)707-711
Number of pages5
JournalNucleosides and Nucleotides
Volume7
Issue number5-6
DOIs
StatePublished - 1 Oct 1988

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