387
Views
2
CrossRef citations to date
0
Altmetric
Original Articles

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

, &
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.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.