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Original Articles

Design and Facile Synthesis of New Dinucleotide Cap Analog Containing Both 2′ and 3′-OH Modification on M7Guanosine Moiety

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Pages 611-619 | Received 14 Jan 2015, Accepted 13 Apr 2015, Published online: 07 Aug 2015
 

Abstract

The first example of the synthesis of new dinucleotide cap analog containing 2,3-diacetyl group on m7guanosine moiety is described. The desired modified cap analog, m7,2,3–diacetylG[5]ppp[5]G has been obtained by the coupling reaction of triethylamine salt of m7,2,3–diacetylGDP with ImGMP in presence of ZnCl2 as a catalyst in 62% yield with high purity. The structure of new cap analog has been confirmed by 1H and 31P NMR and mass data.

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