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I. PROGRESS IN SECOND GENERATION OLIGOMER THERAPEUTICS

A Convenient Synthesis of Deoxynebularine Phosphoramidite

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Pages 937-939 | Published online: 16 Aug 2006
 

Abstract

Enzyme catalysis by a cell free preparation from Lactobacillus leichmannii is used to accomplish the transformation of thymidine to deoxynebularine in the presence of purine. The resulting mixture of nucleosides is then converted to their 5′-dimethoxytrityl derivatives which are easily separated using conventional chromatography. Phosphitylation of the 5′-dimethoxytrityl-deoxynebularine then gives the phosphoramidite derivative suitable for incorporation into oligonucleotides.

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