Solution-phase synthesis of oligodeoxyribonucleotides using the H-phosphonate method with N-unprotected 5′-phosphite monomers. Issue 60 (25th November 2021)

• Record Type: Journal Article
• Authors: Matsuda, Hiromasa; Yoshida, Erina; Shinoda, Takaaki; Sato, Kazuki; Hara, Rintaro Iwata; Wada, Takeshi
• Is Part Of: RSC advances. Volume 11:Issue 60(2021)
• Page Start: 38094
• Page End: 38107
• Publication Date: 2021-11-25
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d1ra06619f
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : A new strategy for a solution-phase synthesis of oligodeoxyribonucleotides with 5′-phosphite monomers synthesized in a single step from unprotected 2′-deoxyribonucleosides. Abstract : Recent advances in nucleic acid therapeutics increase the requirements for developing efficient methods for the chemical synthesis of oligodeoxyribonucleotides (ODNs). In this study, we report a new approach for the solution-phase synthesis of ODNs using the H -phosphonate method with N -unprotected 5′-phosphite monomers. The 5′-phosphite monomers are synthesized in a single step from unprotected 2′-deoxyribonucleosides using 5′- O -selective phosphitylation and can be applied to the synthetic cycle of the H -phosphonate method. We synthesized four kinds of 5′-phosphite monomers and then optimized the conditions for the condensation between the 3′-hydroxy groups of the 5′-phosphite monomers and the H -phosphonate monoesters. As a result of various investigations, solution-phase synthesis of trithymidine diphosphate (TTT) and tetramers containing four kinds of nucleobases was achieved according to the procedure consisting of repeated condensation, deprotection, and purification using simple extraction or precipitation.