Nucleoside bearing boron clusters and their phosphoramidites – building blocks for modified oligonucleotide synthesis. (2nd December 2014)

• Record Type: Journal Article
• Authors: Matuszewski, Michał; Kiliszek, Agnieszka; Rypniewski, Wojciech; Lesnikowski, Zbigniew J.; Olejniczak, Agnieszka B.
• Is Part Of: New journal of chemistry. Volume 39:Number 2(2015:Feb.)
• Page Start: 1202
• Page End: 1221
• Publication Date: 2014-12-02
• Subjects: Chemistry -- Periodicals; Chimie -- Périodiques; 540
• DOI: 10.1039/c4nj01096e
• Languages: English
• ISSNs: 1144-0546

Abstract

Abstract : Synthesis of four canonical nucleoside- closo -/ nido -carborane conjugates, their phosphoramidites, their electrochemical characteristics and the first example of the X-ray structure of a nucleoside-boron cluster conjugate. Abstract : This paper describes a general method for the synthesis of four canonical nucleosides T, dC, dA and dG and their phosphoramidites suitable for automated synthesis of DNA modified with a carborane cage. A boron cluster in the form of an electroneutral, lipophilic 1, 2-dicarba- closo -dodecaborane (C2 B9 H11 ) or negatively charged, redox-active 7, 8-dicarba- nido -undecaborate ion (C2 B9 H12 (−1)) was used as a modifying unit. The method is based on the "click chemistry" type Huisgen–Sharpless–Meldal reaction. All boron cluster-nucleoside conjugates have been characterized electrochemically; they have shown different redox potentials allowing for selective electrochemical identification of individual nucleosides in the mixture. There is also the first description of the crystallographic structure of the boron cluster-nucleoside conjugate: N 3 -{[( o -carboran-1-yl)propyl]-1 N -1, 2, 3-triazol-4-yl}methylenethymidine.